Care
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Akileine dermo akilortho cream for prosthesis tube 75 ml
AKILEINE Dermo Akilortho Cream for Denture Tb 75 ml product description AKILEINE Dermo Akilortho Cream for Denture Tb 75 ml Do you wear dentures and experience discomfort or pain due to the friction caused by the denture rubbing against your gums? AKILEINE Dermo Akilortho cream for denture Tb 75 ml can help alleviate these issues. The cream contains natural active ingredients such as arnica, sage, and ginger which provide Care and analgesic properties. These ingredients also have antiseptic and antioxidant properties which help to protect and heal the delicate gum tissue. The cream is easy to apply and does not leave any residue or greasy feeling in your mouth. Simply apply a small amount of cream on the areas of your gums where the denture rubs against and massage gently. Repeat as needed throughout the day. AKILEINE Dermo Akilortho cream for denture Tb 75 ml is suitable for anyone who wears dentures and experiences discomfort or pain. It is also suitable for those who have sensitive gums or allergies to certain chemicals or ingredients commonly found in other denture creams. Don't let denture discomfort or pain ruin your day. Try AKILEINE Dermo Akilortho cream for denture Tb 75 ml today and experience the relief and comfort you deserve...
26.74 USD
Algifor-l film-coated tablets 200 mg 20 pcs
The Algifor-L 200 film-coated tablet contains the active ingredient ibuprofen in the form of ibuprofen lysinate. It has pain-relieving, fever-reducing and Care properties. Ibuprofen lysinate shows the same properties as ibuprofen, but differs in its higher water solubility. Algifor-L 200 is suitable for short-term Care, i. for a maximum of 3 days Care of: Pain in the area of joints and ligaments, Back pain, Headache, Toothache, Pain during of menstrual bleeding, Pain after injury, Fever with flu-like illnesses. Ref:-approved patient information Algifor-L® 200 film-coated tabletsVERFORA SAWhat is Algifor-L 200 and when is it used?..
35.09 USD
Algifor-l forte film-coated tablets 400 mg 10 pcs
The Algifor-L forte 400 film-coated tablet contains the active ingredient ibuprofen in the form of ibuprofen lysinate. It has pain-relieving, fever-reducing and Care properties. Ibuprofen lysinate shows the same properties as ibuprofen, but differs in its higher water solubility. Algifor-L forte 400 is suitable for short-term Care, i. for a maximum of 3 days Care of: Pain in the area of joints and ligaments, Back pain, Headache, Toothache, Pain during of menstrual bleeding, Pain after injury, Fever with flu-like illnesses. Ref:-approved patient information Algifor-L® forte 400 film-coated tabletsVERFORA SAWhat is Algifor-L forte 400 and when is it used?The Algifor-L forte 400 film-coated tablet contains the active ingredient ibuprofen as ibuprofen lysinate. It has pain-relieving, fever-reducing and Care properties. Ibuprofen lysinate shows the same properties as ibuprofen, but differs in its higher water solubility. Algifor-L forte 400 is suitable for short-term Care, i. for a maximum of 3 days Care of: Pain in the area of joints and ligaments,Back pain,Headache,Toothache,Pain during of the menstrual period,Pain after injury,Fever with flu-like illnesses.When may Algifor-L forte 400 not be used?If you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other Cares or Wellness care for medicines, so-called non-steroidal Care drugs;if you are pregnant or breastfeeding (see also chapter "Can Algifor-L forte 400 be taken during pregnancy or while breastfeeding?");if you have an active stomach and/or duodenal ulcers or gastrointestinal bleeding;in chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in severe impairment of liver or kidney function;in severe cardiac insufficiency;for the Care of pain after coronary bypass surgery on the heart (or Use of a heart-lung machine);in the case of a varicella infection (chickenpox infection);in children under the age of 12. Algifor-L forte 400 has not been tested for use in children under the age of 12.When should caution be taken when taking Algifor-L forte 400?During Care with Algifor-L forte 400, mucosal ulcers, rarely bleeding or, in isolated cases, perforations (stomach or intestinal perforations) may occur in the upper gastrointestinal tract. These complications can occur at any time during Care, even without warning symptoms. To reduce this risk, your doctor will prescribe the smallest effective dose for the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine or if you have an infection - see below under «Infections». For certain Cares, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found with long-term Care. This risk can also be slightly increased with Algifor-L forte 400 at a high dose (2400 mg/day). However, no increase in this risk was found at the usual dosage (maximum 1200 mg/day). If you have already had a heart attack, stroke or venous thrombosis, the use of Algifor-L forte 400 in high doses is no longer recommended. Do not exceed the recommended dose or duration of Care and always tell your doctor if you have had a heart attack, stroke or thrombosis in a vein, or if you have risk factors (such as high blood pressure, diabetes (sugar diabetes), high blood fat levels, Smoking). Your doctor will decide whether you can still use Algifor-L forte 400 and which dose is suitable for you. Taking Algifor-L forte 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema). Tell your doctor if you have heart or kidney disease, if you are taking medicines to treat high blood pressure (e.g. diuretics, ACE inhibitors) or if you lose more fluids, e.g. through heavy sweating. This medicine can affect your ability to react, drive and use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of gastric or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients suffering from Wellness care for, chronic inflammation of the nasal mucosa (chronic runny nose), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagen diseases). Serious skin reactions have been reported in association with Care with non-steroidal Care drugs. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, including fever, mucous membrane lesions, blisters or any other sign of allergy, you should stop using Algifor-L forte 400 and seek medical attention immediately, as these may be the first signs of a very serious skin reaction ( see the section «What side effects can Algifor-L forte 400 have?»). Algifor-L forte 400 should not be used if you have chickenpox. InfectionsAlgifor-L forte 400 can mask signs of infections such as fever and pain. It is therefore possible that Algifor-L forte 400 delays adequate Care of the infection, which can lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately. Tell your doctor if you have recently received Care for an abortion. Tell your doctor if you are being treated with medicines such as blood thinners (e.g. low-dose acetylsalicylic acid), diuretics (water tablets), ACE inhibitors or β-blockers (medicines for high blood pressure and heart failure), antibiotics , certain medicines against fungal infections (e.g. voriconazole or fluconazole), immunosuppressants (preparations against transplant rejection), herbal extract from Ginkgo biloba, medicines for high blood sugar, against AIDS, epilepsy and depression. Nonsteroidal Care drugs such as ibuprofen and the medicines listed above can interact. In particular, long-term Care with Algifor-L forte 400 may reduce the cardioprotective effect of low-dose acetylsalicylic acid. Acetylsalicylic acid or other pain relievers should not be taken at the same time as ibuprofen as the risk of side effects may be increased. Side effects, particularly affecting the gastrointestinal tract or the central nervous system, can be increased if alcohol is consumed at the same time. Prolonged use of Cares can cause headaches. Do not treat them with an increased dose of the drug, but inform your doctor, Ref: or your doctor, Ref:. Elderly patientsElderly patients are more likely to experience side effects after using non-steroidal Care drugs, especially bleeding and perforation in the stomach and intestines. Therefore, particularly careful medical supervision is required in elderly patients. Inform your doctor, Ref: or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!) or using them externally. Can Algifor-L forte 400 be used during pregnancy or breastfeeding?PregnancyYou should If you are pregnant or planning a pregnancy, you should only take Algifor-L forte 400 after consulting your doctor. You should not take Algifor-L forte 400 unless it is clearly necessary and prescribed by a doctor. If taken during the first 6 months of pregnancy, the dose should be kept as low and the duration of Care as short as possible. Taking nonsteroidal Care drugs (NSAIDs) after the 20th week of pregnancy may harm your unborn baby. If you have to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the fetal heart. Algifor-L forte 400 must not be taken in the last third of pregnancy. BreastfeedingAlgifor-L forte 400 should not be taken while breastfeeding unless your doctor has given you express permission to do so. How do you use Algifor-L forte 400?Algifor-L forte 400 film-coated tablets should be taken with or after meals. The film-coated tablets should be swallowed with a glass of water or other liquid. The film-coated tablets are to be swallowed whole and should not be chewed, broken, crushed or sucked to prevent mouth discomfort and throat irritation. The lowest effective dose should be used for the shortest time necessary to relieve symptoms. If you have an infection, consult a doctor immediately if symptoms (e.g. fever and pain) persist or worsen (see «When should you take Algifor-L forte 400 with caution?»). Adults and adolescents from 12 years of age: take 1 film-coated tablet with plenty of liquid. A gap of 4 to 6 hours should be observed before the next dose. In the case of pain during the menstrual period, it is recommended to start Care with 1 Algifor-L forte 400 tablet at the first sign of the symptoms. Maximum daily dose: Do not take more than 3 film-coated tablets in a 24-hour period, unless prescribed by a doctor. Do not use Algifor-L forte 400 for more than 3 days and only to treat the symptoms listed above. If the symptoms increase despite taking Algifor-L forte 400 or if the painful area becomes red or swollen, consult your doctor. A serious illness can be the cause. Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. The tablets are not suitable for half-dose dosing by splitting. Children under the age of 12: Algifor-L forte 400 must not be used in children under the age of 12. The use and safety of Algifor-L forte 400 in children under the age of 12 has not yet been tested. Follow the dosage given in the package leaflet or as prescribed by your doctor. If you have taken more Algifor-L forte 400 than you should, or if children have accidentally taken the medicine, always contact a doctor for an assessment of the risk and advice on further Care to get. Symptoms can include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported. If you forget to take a dose, do not take more than the usual recommended amount next time. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Algifor-L forte 400 have?The following side effects can occur when taking Algifor-L forte 400. They are listed by frequency: Common (affects 1 to 10 users in 100)gastrointestinal disorders such as indigestion, Wellness care for, nausea, vomiting, Wellness care for, upper abdominal pain, Flatulence, tarry stool, vomiting blood, gastrointestinal bleedingCentral nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizzinessAcute skin rashUncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosaHypersensitivity reactionsInsomnia , feeling anxiousVisual disturbances (the visual disturbances are usually reversible if Care is stopped)Ringing in the ears, hearing loss, dizzinessWellness care for, spasms of the muscles of the airways and shortness of breath. Patients with heart failure are at risk of acute pulmonary edema (water lung)FatigueRare (affects 1 to 10 users in 10,000)Aseptic meningitis (meningitis)Angina, high fever, swelling of the lymph nodes in the neck areaAllergic reactions, symptoms of lupus erythematosus (butterfly plexus) , Wellness care forDepression, confusional states"Tingling" of the skin, drowsinessIrreversible visual disturbance or poor eyesightInflammation of the stomach lining, stomach and intestinal ulcers, ulcers of the oral mucosa, gastric and intestinal perforationsHepatitis, jaundice, liver dysfunctionHives, itching, bleeding in the skin, swelling of the skin and mucous membranes, sensitivity to light Various kidney disorders such as kidney dysfunction with fluid retention in the tissues and kidney failureGeneral swellingVery rare (affects less than 1 in 10' 000 users)Psychotic statesHeart failure, heart attackHigh blood pressureInflammation of the pancreasLiver failureSevere allergic skin reactions with blistering and/or widespread detachment of the skin.Frequency not known (can be estimated from the available data cannot be estimated)A serious skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include a rash, fever, swollen lymph nodes, and an increase in eosinophils (a type of white blood cell).worsening of colitis or Crohn's diseasea red, scaly, widespread rash with bumps under the skin and blisters accompanied by fever, primarily on the skin folds, trunk and upper extremities (acute generalized pustular rash). Stop using Algifor-L forte 400 if you develop these symptoms and seek medical attention immediately.If you get any side effects, talk to your doctor or Ref: or druggists or your doctor, Ref: or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The Care product may only be used up to the date marked «EXP» on the container. Storage instructionsStore the medicine at room temperature (15-25 °C) and out of the reach of children. Your doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does Algifor-L forte 400 contain?1 film-coated tablet Algifor-L forte 400 contains: Active ingredients400 mg ibuprofen as ibuprofen lysinate ExcipientsMicrocrystalline cellulose, crospovidone, magnesium stearate, polyvinyl alcohol, titanium dioxide, talc, macrogol 3350, soy lecithin Approval number55766 (Ref:). Where can you get Algifor-L forte 400? What packs are available?In pharmacies and drugstores, without a doctor's Ref:. Algifor-L forte 400: pack of 10 film-coated tablets. Authorization holderVERFORA SA, 1752 Villars-sur-Glâne. This leaflet was last checked by the Medicines Agency (Ref:) in November 2022. ..
35.09 USD
Alka seltzer effervescent tablets 10 x 2 pcs
Alka-Seltzer contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and Care properties. Alka-Seltzer is suitable for short-term Care, i. for the maximum 3-day Care of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic Care of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's Ref: and only as a second-line drug (see «When should caution be taken when taking Alka-Seltzer?»). Ref:-approved patient informationAlka-Seltzer®, effervescent tablets Bayer (Schweiz) AG What is ALKA-SELTZER and when is it used?Alka-Seltzer contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and Care properties. Alka-Seltzer is suitable for short-term Care, i. for the maximum 3-day Care of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic Care of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's Ref: and only as a second-line drug (see «When should caution be taken when taking Alka-Seltzer?»). What should be considered?Alka-Seltzer should not be used for more than 3 days, unless prescribed by a doctor. Cares should not be taken regularly over a long period of time without medical supervision. Long-lasting pain requires a medical check-up. The dosage specified or prescribed by the doctor must not be exceeded. It's also important to remember that long-term use of Cares can itself contribute to headache persistence. Long-term use of Cares, especially when taking a combination of several Cares, can lead to permanent kidney damage with the risk of kidney failure. When should ALKA-SELTZER not be used?You should not use Alka-Seltzer in the following cases: If you are allergic to any of the ingredients or have had shortness of breath or an allergy-like skin reaction after taking acetylsalicylic acid, other salicylates or other pain or Wellness care for medicines called non-steroidal Care drugs. in the case of active stomach and/or duodenal ulcers or stomach/intestinal bleeding,In the case of chronic intestinal inflammation (Crohn's disease, ulcerative colitis).If you have a pathologically increased tendency to bleed.Severely impaired liver or kidney function.Severe heart failure.For the Care of pain after coronary bypass surgery on the heart (or use of a heart-lung machine).If you have to take methotrexate at a dose of more than 15 mg per week at the same time.In children under 12 years of age.When is caution required when using ALKA-SELTZER?During Care with Alka-Seltzer, ulcers in the mucous membranes of the upper gastrointestinal tract, rarely bleeding or in individual cases perforations (gastrointestinal breakthroughs) occur. These complications can occur at any time during Care, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine. Elderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. You should only take Alka-Seltzer on Ref: and under medical supervision in the following situations:If you are currently being treated by a doctor for a serious illness. If you have previously had a stomach or duodenal ulcer.If you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors ) or in case of increased fluid loss, e.g. through heavy sweating; taking Alka-Seltzer can affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema).If you have liver problems. If you are being treated with anticoagulants (blood thinners, anticoagulants) or suffer from a blood clotting disorder;If you suffer from Wellness care for;If you are taking antirheumatic medicines or other Cares.For Wellness care for, hives, nasal polyps, hay fever or other allergies, for a rare hereditary disease of the red blood cells, the so-called "glucose-6-phosphate dehydrogenase deficiency" and for Care with anticoagulants (“blood thinners”, anticoagulants) or blood pressure lowering agents (antihypertensives) should only be taken according to the doctor’s strict instructions. Patients who have to eat a low-salt diet on medical advice (e.g. kidney disease, severe heart failure) should only use Alka-Seltzer effervescent tablets in exceptional cases because of their high sodium content. Adolescents from the age of 12 with fever, flu, chickenpox or other viral diseases may only take Alka-Seltzer on the doctor's instructions and only as a second-line remedy. If these diseases lead to disorders of consciousness with vomiting or after they have disappeared, the doctor should be consulted immediately. The simultaneous and prolonged use of Alka-Seltzer can increase the effect of cortisone preparations, anticonvulsants (antiepileptics), blood thinners, digoxin and lithium preparations against depression. There may be an increase in the undesirable effects of these medicines. The effect of gout medicines (Probenecid and Sulfinpyrazone), water tablets (diuretics) and medicines for high blood pressure can be reduced. The use of anti-rheumatic drugs or methotrexate (which is taken for chronic polyWellness care for, for example; see also the section "When should Alka-Seltzer not be used?") may result in an increase in the undesirable effects. Alka-Seltzer can increase the risk of bleeding if you take cortisone preparations, alcohol or drugs from the group of so-called serotonin reuptake inhibitors for depression. If Alka-Seltzer and antidiabetics (e.g. insulin, sulfonylureas) are taken at the same time, the blood sugar level can drop. Even in small doses, acetylsalicylic acid reduces the excretion of uric acid. This can trigger gout in patients who already have low uric acid excretion. Caution is required in conditions with an increased risk of bleeding (e.g. menstrual bleeding or injuries). There may be an increased tendency to bleed, especially during and after surgical interventions (including minor interventions such as tooth extraction). Your doctor or dentist should be asked or informed about taking it before surgery. Serious skin reactions have been reported in association with Care with non-steroidal Care drugs. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, including fever, mucosal lesions, blisters or any other sign of allergy, you should stop using Alka-Seltzer and seek medical attention immediately, as these may be the first signs of a very serious skin reaction (see section «What side effects can Alka-Seltzer have?» ). Tell your doctor, Ref: or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!).Can ALKA-SELTZER be taken while pregnant or breastfeeding?PregnancyYou should not take Alka-Seltzer, es unless it is clearly necessary and prescribed by a doctor. If taken during the first 6 months of pregnancy, the dose should be kept as low and the duration of Care as short as possible. Taking nonsteroidal Care drugs (NSAIDs) after the 20th week of pregnancy can harm your unborn baby. If you have to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the fetal heart. If you are pregnant or planning to become pregnant, you should only take Alka-Seltzer after consulting your doctor. Alka-Seltzer should not be taken during the last trimester of pregnancy. BreastfeedingAlka-Seltzer should not be taken while breastfeeding unless your doctor has given you permission to do so. How do you use ALKA-SELTZER?Adults and young people aged 12 and over and weighing more than 40 kg: 1-2 effervescent tablets A daily dose of 8 tablets must not be exceeded for adults. Alka-Seltzer must always be dissolved in water. The intake can be repeated about every 4 hours up to 4 doses within 24 hours. It should not be taken on an empty stomach. Adolescents from the age of 12 may only take Alka-Seltzer if prescribed by a doctor and only as a second-line drug. Alka-Seltzer should not be used in children under 12 years of age. In the event of uncontrolled intake (overdose), consult a doctor immediately. Ringing in the ears and/or sweating can be an indication of an overdose. Follow the dosage given in this leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can ALKA-SELTZER have?Stomach problems can occur as side effects. In rare cases, hypersensitivity reactions such as swelling of the skin and mucous membranes (e.g. blocked nose), skin rashes, Wellness care for, shortness of breath and gastrointestinal ulcers and gastrointestinal bleeding, bruising, nosebleeds or bleeding gums may occur. Serious bleeding, which in isolated cases can be potentially life-threatening, has also been reported very rarely. Changes in the intestinal wall have been reported. If signs of a hypersensitivity reaction occur, the drug should be discontinued and the doctor consulted. If the stool turns black or there is blood in the vomit during Care, the drug should be discontinued and the doctor consulted immediately. Rarely, dizziness, headaches, blurred vision and confusion occur. Frequency not known: A serious skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include a rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell). If you notice any side effects that are not described here, you should inform your doctor, Ref: or druggist.What else is to be done note? Store at room temperature (15 - 25°C) and protect from moisture. The Care product should be kept out of the reach of children! The Care product may only be used up to the date marked «EXP» on the container. Your doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does ALKA-SELTZER contain?Active ingredients1 effervescent tablet contains 324 mg acetylsalicylic acid ExcipientsFlavourings, sodium saccharate, preservative: sodium benzoate (E 211) and other excipients. Approval number08671 (Ref:) Where can you get ALKA-SELTZER? What packs are available?In pharmacies and drugstores, without a doctor's Ref:. Packs of 20 effervescent tablets. Authorization holderBayer (Switzerland) AG, 8045 Zurich. This leaflet was last checked by the drug authority (Ref:) in February 2023. ..
46.69 USD
Aromasan borage oil organic 50 ml
AROMASAN Borage Oil Bio 50ml Our AROMASAN Borage Oil Bio is a pure and natural oil that is cold-pressed from the seeds of the borage plant. Borage Oil contains high levels of gamma-linolenic acid (GLA) which is an omega-6 fatty acid that is known to have Care properties. This makes it a great choice for those with inflammatory skin conditions such as eczema, psoriasis, and acne. Not only is it great for skin health, but it also has benefits for overall health. Borage Oil has been shown to help lower cholesterol, reduce inflammation in the body, and support cardiovascular health. Our Borage Oil is certified organic and has been ethically sourced to ensure the highest quality product possible. It is also vegan-friendly and cruelty-free. Directions for Use: Add a few drops to your favorite moisturizer for added hydration and Care benefits. Massage into the skin to help reduce inflammation and soothe irritated skin. Add a few drops to your bath for a relaxing and moisturizing experience. Ingredients: 100% pure cold-pressed borage oil (Borago officinalis) Disclaimer: Our products are not intended to diagnose, treat, Care, or prevent any disease. Please consult with a healthcare professional before starting any new supplement or skincare routine. ..
59.07 USD
Aromasan ginger ether/oil organic 15 ml
Elevate your well-being with Aromasan's organic ginger ether/oil. Carefully crafted with nature's finest ingredients, this 15 ml bottle is a powerhouse of wellness benefits. Use it in aromatherapy to invigorate your senses or dilute it for topical application to soothe muscles and joints. Ginger is renowned for its Care properties and digestive support, making it a versatile addition to your natural remedies collection. Treat yourself to the soothing essence of organic ginger and experience the holistic benefits of phytotherapy with Aromasan...
75.43 USD
Aromasan wintergreen ether/oil 30 ml
Aromasan Wintergreen Äth/Oil 30 mL If you're looking for a natural Wellness care for muscle pain and inflammation, look no further than Aromasan Wintergreen Äth/Oil 30 mL. Wintergreen essential oil, or Gaultheria procumbens, has been used for centuries to alleviate pain and reduce inflammation naturally. This oil is derived from the leaves of the wintergreen plant and has a minty scent that can help invigorate the mind and body. Benefits of Aromasan Wintergreen Äth/Oil Reduces muscle pain and inflammation Improves circulation Relieves tension and stress Alleviates headaches and Wellness care fors How to Use Aromasan Wintergreen Äth/Oil Wintergreen essential oil should never be used undiluted on the skin as it can cause irritation. To use this oil, dilute it with a carrier oil such as coconut or jojoba oil. Aromasan Wintergreen Äth/Oil can be used topically or in aromatherapy. To use topically, mix a few drops with a carrier oil and apply to the affected area. For aromatherapy, add a few drops to a diffuser or humidifier to fill your room with the scent. Why Choose Aromasan Wintergreen Äth/Oil Aromasan Wintergreen Äth/Oil is made from high-quality, pure wintergreen essential oil that is rigorously tested for purity and potency. This product is free from additives, fillers, and synthetic fragrances, making it a natural alternative to conventional Care medications. Plus, the convenient 30 mL bottle makes it easy to take with you on the go. Order Aromasan Wintergreen Äth/Oil Today If you're looking for a natural Wellness care for muscle pain and inflammation, Aromasan Wintergreen Äth/Oil 30 mL is the perfect solution. Order yours today and experience the natural Wellness care for power of wintergreen essential oil. ..
43.10 USD
Aspirin chewable 500 mg 20 pcs
Aspirin contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and Care properties. Aspirin chewable tablets are suitable for short-term Care, i. for the maximum 3-day Care of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic Care of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's Ref: and only as a second-line drug (see "When should you be careful when taking aspirin?"). Ref:-approved patient informationAspirin® chewable tabletsBayer (Schweiz) AGWhat is aspirin and when is it used?Aspirin contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and Care properties. Aspirin chewable tablets are suitable for short-term Care, i. for the maximum 3-day Care of mild to moderately severe, acute pain (headache, toothache, joint and ligament pain, back pain) and for the symptomatic Care of fever and/or pain associated with colds. Adolescents from 12 years of age only with a doctor's Ref: and only as a second-line drug (see "When should you be careful when taking aspirin?"). What should be considered?Aspirin should not be used for more than 3 days unless prescribed by a doctor. Cares should not be taken regularly over a long period of time without medical supervision. Long-lasting pain requires a medical check-up. The dosage specified or prescribed by the doctor must not be exceeded. It's also important to remember that long-term use of Cares can itself contribute to headache persistence. Long-term use of Cares, especially when taking several Cares in combination, can lead to permanent kidney damage with the risk of kidney failure. When shouldn't aspirin be taken/used?You shouldn't use aspirin in the following cases: If you are allergic to any of the ingredients or have had shortness of breath or an allergy-like skin reaction after taking acetylsalicylic acid, other salicylates or other pain or Wellness care for medicines called non-steroidal Care drugs. If you suffer from a stomach and/or duodenal ulcer or have gastrointestinal bleeding.If you have chronic intestinal inflammation (Crohn's disease, ulcerative colitis).If you have a have a pathologically increased tendency to bleed.Severely impaired liver or kidney function.Severe heart failure.For the Care of pain after coronary bypass surgery on the Heart (or use of a heart-lung machine).If you have to take methotrexate at a dose of more than 15 mg per week at the same time.If you are pregnant or breastfeeding (See also the section «Can aspirin be taken during pregnancy or breastfeeding?»).For children under the age of 12.When is caution required when taking / using aspirin? During Care with aspirin, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (gastrointestinal perforations) may occur . These complications can occur at any time during Care, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine. Elderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. You may only take aspirin with a Ref: and under medical supervision in the following situations: If you are currently being treated by a doctor for a serious illness.If you have previously suffered from a stomach or duodenal ulcer.If you have heart disease or have kidney disease or increased fluid loss, e.g. due to heavy sweating, Wellness care for or after major surgery; taking aspirin can affect how your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema).If you have liver problems.If you have Wellness care for, hives, nasal polyps, hay fever or other allergies, if you have a rare hereditary disease of the red blood cells, the so-called "glucose-6-phosphate dehydrogenase deficiency" and if you are being treated with anticoagulants ("blood thinners", Anticoagulants) or blood pressure lowering agents (antihypertensives) should only be taken according to the strict instructions of the doctor. Adolescents from the age of 12 with fever, flu, chickenpox or other viral diseases may only take aspirin as directed by their doctor and only as a second-line drug. If these diseases lead to disorders of consciousness with vomiting or after they have disappeared, the doctor should be consulted immediately. The effect of cortisone preparations, antispasmodics (antiepileptics), blood thinners, digoxin and lithium preparations against depression can be increased with simultaneous and prolonged use of aspirin. There may be an increase in the undesirable effects of these medicines. The effect of gout medicines (Probenecid and Sulfinpyrazone), water tablets (diuretics) and medicines for high blood pressure can be reduced. The use of anti-rheumatic drugs or methotrexate (which is taken, for example, for chronic polyWellness care for; see also the section “When should aspirin not be used?”) may result in an increase in the undesirable effects. Aspirin can increase the risk of bleeding if you take cortisone preparations, alcohol or drugs from the group of so-called serotonin reuptake inhibitors for depression. If you take aspirin and antidiabetics (e.g. insulin, sulfonylureas) at the same time, the blood sugar level can drop. Even in small doses, acetylsalicylic acid reduces the excretion of uric acid. This can trigger gout in patients who already have low uric acid excretion. In conditions with an increased risk of bleeding (e.g. menstrual bleeding or injuries), caution is required, especially during and after surgical interventions (including minor interventions such as tooth extractions) there may be an increased tendency to bleed. Your doctor or dentist should be asked or informed about taking it before surgery. This Care product contains 16.5 mg aspartame per tablet. Aspartame is a source of phenylalanine. It can be harmful if you have phenylketonuria (PKU), a rare inherited disorder in which phenylalanine builds up because the body can't break it down enough. This Care product contains less than 1 mmol sodium (23 mg) per tablet, i.e. essentially 'sodium-free'. it is almost «sodium-free». This medicine contains the azo dye sunset yellow FCF (E110). E 110 can cause allergic reactions. This medicine contains fructose. Fructose can damage teeth. This medicine contains sulfur dioxide (E 220). In rare cases, E 220 can cause severe hypersensitivity reactions and bronchial spasms (bronchospasms). This Care product contains small amounts of ethanol (alcohol) in the flavour. The small amount of alcohol in this medicine has no noticeable effects. Serious skin reactions have been reported in association with Care with non-steroidal Care drugs. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, including fever, mucous membrane lesions, blisters, or any other sign of allergy, you should stop taking aspirin and seek medical attention immediately, as these can be the first signs of a very serious skin reaction (see section What Aspirin can have side effects?» ). Tell your doctor, Ref: or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!).Can aspirin be taken/used while pregnant or breastfeeding?PregnancyYou should not take aspirin unless , it is clearly necessary and prescribed by a doctor. If taken during the first 6 months of pregnancy, the dose should be kept as low and the duration of Care as short as possible. Taking nonsteroidal Care drugs (NSAIDs) after the 20th week of pregnancy may harm your unborn baby. If you have to take NSAIDs for more than 2 days, your doctor may need to monitor the amount of amniotic fluid in the womb and the fetal heart. If you are pregnant or planning to become pregnant, you should only take aspirin after consulting your doctor. Aspirin should not be taken during the last trimester of pregnancy. BreastfeedingAspirin should not be taken while breastfeeding unless your doctor has given you permission to do so. How do you use aspirin?Adults and adolescents aged 12 and over and heavier than 40 kg: 1-2 chewable tablets, if necessary every 4th day - Repeat for 8 hours. Up to a maximum of 6 chewable tablets daily. Chew the aspirin tablets in your mouth and swallow with or without water. It should not be taken on an empty stomach. Adolescents 12 years and older may only take aspirin with a doctor's Ref: and only as a second-line drug. Children under the age of 12: Aspirin chewable tablets are not suitable for children under the age of 12 because of the high active ingredient content. In the event of uncontrolled intake (overdose), consult a doctor immediately. Ringing in the ears and/or sweating can be an indication of an overdose. Follow the dosage given in this leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can aspirin have?Very common (affects more than 1 in 10 people)Micro bleeding ( 70%). Common (affects 1 to 10 users in 100)Stomach disorders. Uncommon (affects 1 to 10 users in 1000)Wellness care for, shortness of breath, upper abdominal discomfort, nausea, vomiting, diarrhoea. Rare (affects 1 to 10 users in 10,000)Coagulation deficiency (lack of blood platelets), lack of white blood cells, lack of blood cells (aplastic anaemia), iron deficiency , increased risk of bleeding (e.g. gastrointestinal bleeding, bruising, nosebleeds, bleeding gums, bleeding in the urine and genital organs, bleeding during operations, bleeding in the brain). Hypersensitivity reactions, such as swelling of the skin and mucous membranes (e.g. blocked nose), skin rashes (Steven Johnson syndrome, toxic epidermal necrolysis), nettle fever, hay fever, spasms of the airways, Quincke's edema (facial swelling), drop in blood pressure. Stomach/intestinal ulcers. Dizziness, headache, tinnitus (ringing in the ears), hearing loss, visual disturbances, confusional states. Hypoglycaemia, disturbance of the acid-base balance. Liver dysfunction. Kidney dysfunction. Very rare (affects less than 1 in 10,000 people treated)Severe bleeding, which in isolated cases can be life-threatening, has also been reported very rarely. Elevated transaminases (liver values). Reye's syndrome (disease affecting the brain and liver in children). If signs of a hypersensitivity reaction occur, the drug should be discontinued and your doctor consulted. If the stool turns black or there is blood in the vomit during Care, the drug should be discontinued and the doctor consulted immediately. Frequency not known (cannot be estimated from the available data)Changes in the intestinal wall, especially with long-term use, as well as Wellness care for and acute kidney failure have been reported. Frequency not known: A serious skin reaction known as DRESS syndrome can occur. Symptoms of DRESS include a rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell). If you get any side effects, talk to your doctor, Ref: or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?Shelf lifeThe Care product may only be used up to the date marked on the container with « EXP» can be used. Storage instructionsStore at room temperature (15-25°C), protected from moisture and out of the reach of children. Further informationYour doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does aspirin contain?Active ingredients1 chewable tablet contains 500 mg acetylsalicylic acid ExcipientsMannitol (E 421), corn starch, calcium stearate, sunset yellow FCF (E110), heavy basic magnesium carbonate, pregelatinized starch, citric acid, ascorbic acid, carmellose sodium, sodium carbonate , Aromatics: orange, tangerine (contains ethanol), and dry flavor (contains fructose and sulfur dioxide (E220)), aspartame (E951). Approval number49526 (Ref:). Where can you get aspirin? What packs are available?In pharmacies and drugstores, without a doctor's Ref:. Packs of 10 and 20 chewable tablets. Authorization holderBayer (Switzerland) AG, 8045 Zurich. This leaflet was last checked by the drug authority (Ref:) in February 2023. ..
34.80 USD
Aspirin instant tablets 500 mg 6 bags 2 pieces
Aspirin 500 contains the active ingredient acetylsalicylic acid. It has pain-relieving, fever-reducing and Care properties. Aspirin 500 effervescent tablets are used in adults and adolescents aged 12 and over and weighing more than 40 kg for the symptomatic Care of acute headaches. Aspirin 500 effervescent tablets are suitable for short-term Care, i. for a maximum of 3 days of Care. Adolescents from the age of 12 only with a doctor's Ref: and only as a second-line drug (see "When should you be careful when taking Aspirin 500?") Ref:-approved patient informationAspirin® 500, effervescent tabletsBayer (Schweiz) AGWhat is Aspirin 500 and when is it used?..
31.38 USD
Assan thermo cream tube 100 g
Assan thermo cream has Care and analgesic properties as well as circulation-enhancing and warming properties and accelerates the regression of swelling. Assan thermo cream does not smear or grease. Assan thermo cream is suitable as a supportive measure for the local Care of rheumatic complaints of the musculoskeletal system, including muscular pain such as muscle tension, stiff neck and lumbago.T Ref:-approved patient informationAssan® thermo CremePermamed AGWhat is Assan thermo Creme and when is it used?Assan thermo cream has Care and pain-relieving properties as well as circulation-enhancing and warming properties and accelerates the regression of swelling. Assan thermo cream does not smear or grease. Assan thermo cream is suitable as a supportive measure for the local Care of rheumatic complaints of the musculoskeletal system, including muscular pain such as muscle tension, stiff neck and lumbago.T When should Assan thermo cream not be used?Assan thermo cream should not be used if you are hypersensitive to any of the ingredients or to other pain-relieving and Care substances.Do not apply Assan thermo cream to the eyes, mucous membranes, open wounds or damaged skin.Assan thermo cream should not be combined with bathing therapies.With known heparin-induced/associated thrombocytopenia (HIT, lack of blood platelets caused by heparin) Assan thermo cream must not be used. When is caution required when using Assan thermo cream?Assan thermo cream should not be applied to large areas over a long period of time, unless expressly prescribed by a doctor. Tell your doctor, Ref: or druggist if you have already used similar products (Wellness care for ointments) and these have led to allergic reactionssuffer from other diseases,have allergies orothers Taking medicines (including those you bought yourself!) or using them externallyCan Assan thermo cream be used during pregnancy or while breastfeeding?Assan thermo cream should not be used during pregnancy or while breastfeeding, unless specifically prescribed by a doctor. How do you use Assan thermo cream?Adults:Unless otherwise prescribed by the doctor, Assan thermo cream Apply 2-3 times a day in a 5-10 cm long strand to the affected areas and the surrounding skin and massage in. The order center should be free of Cares and cosmetics. Tell your doctor if symptoms worsen or have not improved after 2 weeks. Wash your hands thoroughly after rubbing in Assan thermo cream. Children:The use and safety of Assan thermo cream in children has not yet been tested. Follow the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Assan thermo cream have?In rare cases, skin irritations are possible due to the circulation-enhancing and warming properties. Rarely local allergic reactions. In these cases, Care with Assan thermo cream should be discontinued. If you notice side effects that are not described here, you should inform your doctor, Ref: or druggist. What else needs to be considered?Shelf lifeThe Care product may only be used up to the date marked on the container with « EXP» can be used. Storage instructionsStore Assan thermo cream at room temperature (15-25 °C). Do not ingest and keep out of the reach of children. Further informationYour doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does Assan thermo cream contain?Active ingredients1 g of Assan thermo cream contains the following active ingredients: 35 mg flufenamic acid, 100 mg hydroxyethyl salicylate, 5 mg benzyl nicotinate, 300 IU heparin sodium ExcipientsGlyceryl stearate/PEG-100 stearate, isopropyl palmitate, dimeticone, PEG-2 stearate, PEG-20 methyl glucose sesquistearate, liquid paraffin, methyl glucose sesquistearate, rosemary oil , carbomer 980, pentadecalactone 10%, sodium edetate, caustic soda 30%, purified water. Approval number44615 (Ref:). Where can you get Assan thermo cream? What packs are available? Assan thermo Creme 50 g and 100 g is available in pharmacies and drugstores without a doctor's Ref:. Authorization holderPermamed AG, 4143 Dornach. This leaflet was last checked by the drug authority (Ref:) in April 2019. ..
72.96 USD
Dermacalm d cream tube 20 g
Dermacalm-d is a cooling cream that has a local Care and anti-allergic effect on the skin damage listed below: Skin irritation or mild allergic reactions (with or without itching) caused by contact with detergents, cosmetics, plants, animals or metals (jewellery); Insect bites; Sunburn; Minor burns without open skin. Dermacalm-d has an anti-itching, Care and anti-allergic effect and supports the structure of the damaged skin. The properties of Dermacalm-d are due to hydrocortisone acetate, the most important ingredient in the cream. Hydrocortisone is a naturally occurring in the human body that has an Care effect. If it is applied to the skin, it develops a predominantly local effect. Dermacalm-d also contains dexpanthenol, which is quickly converted into pantothenic acid, a vitamin, by the skin's cells. The pantothenic acid can promote healing of the skin. Ref:-approved patient informationDermacalm-d®, cream Bayer (Schweiz) AG What is Dermacalm-d and when is it used?Dermacalm-d is a cooling cream that has a local Care and anti-allergic effect on the skin damage listed below: Skin irritation or mild allergic reactions (with or without itching) caused by contact with detergents, cosmetics, plants, animals or metal (jewellery);Insect bites;Sunburn;Minor burns without open skin.Dermacalm-d has an anti-itching, Care and anti-allergic effect and supports the structure of the damaged skin. The properties of Dermacalm-d are due to hydrocortisone acetate, the most important ingredient in the cream. Hydrocortisone is a naturally occurring in the human body that has an Care effect. If it is applied to the skin, it develops a predominantly local effect. Dermacalm-d also contains dexpanthenol, which is quickly converted into pantothenic acid, a vitamin, by the skin's cells. The pantothenic acid can promote healing of the skin. What do you need to know?To clean an inflamed or irritated area of skin, use only water as soap may make the irritation worse. Avoid all contact with the substance or material that caused the infection. When not to use Dermacalm-d?Do not use Dermacalm-d if you are allergic to any of its ingredients. Dermacalm-d must not come into contact with the eyes; avoid applying it to the eyelids as well. The cream should not be used if you suffer from fungal infections (e.g. athlete's foot), a viral infection (e.g. cold sores, shingles) or skin reactions following a vaccination; Likewise, application to open wounds and purulent inflammation (e.g. boils, abscesses, acne) should be avoided. When is caution required when using Dermacalm-d?Children under 2 years of age may only use Dermacalm-d under medical supervision. Dermacalm-d should not be applied to large areas of skin or under an impermeable bandage. The cream should not be used for a long time. If there is no improvement after two weeks, you should see a doctor. If symptoms worsen, you should stop Care and consult your doctor. If your symptoms come back within 2 weeks of stopping Care, do not use the cream again without consulting a doctor first, unless your doctor has instructed you to do so. If your symptoms return after they have disappeared, you should seek medical advice before repeating the Care if the redness extends beyond the originally treated area and the skin burns. Inform your doctor, Ref: or druggist if you suffer from any other illnesses,have allergies orother medicines ( also take bought ones) or use them externally!Can Dermacalm-d be used during pregnancy or while breastfeeding?If you are pregnant or want to become pregnant, you may only use Dermacalm-d after consulting your doctor. Dermacalm-d should not be used while breastfeeding. How do you use Dermacalm-d?Apply a thin layer of the cream 1-2 times a day and let it absorb by massaging it in gently. Unless otherwise prescribed by the doctor, a Care with Dermacalm-d should be carried out for a maximum of 2 weeks and not over a large area. In children under the age of 2, Dermacalm-d may only be used under medical supervision. Follow the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Dermacalm-d have?Undesirable effects such as slight burning, itching or increased reddening of the skin can be signs of a hypersensitivity reaction to one or more components of the cream. Hydrocortisone can also cause skin dehydration. With long-term or too frequent use, the risk of the skin becoming increasingly brittle or other skin changes occurring cannot be ruled out. Withdrawal reaction after the end of Care: After continuous use over a long period of time, a withdrawal reaction may occur after the end of Care. You may experience one or more of the following symptoms: reddening of the skin that may extend beyond the treated area, burning or stinging sensation, severe itching, peeling skin, open blisters weeping. If you notice side effects that are not described here, you should inform your doctor, Ref: or druggist. What else needs to be considered?Dermacalm-d is to be kept out of the reach of children and at room temperature (15-25 °C) to keep. The Care product may only be used up to the date marked “EXP” on the container. Your doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does Dermacalm-d contain?1 g cream contains the active ingredients hydrocortisone acetate (5 mg) and dexpanthenol (50 mg) as well as the following auxiliary substances: DL-pantolactone, Cetyl alcohol, paraffin, wool grease (E913), polyoxyl 40 stearate, chlorhexidine dihydrochloride (preservative), water. Approval number51464 (Ref:). Where can you get Dermacalm-d? What packs are available?In pharmacies and drugstores without a doctor's Ref:. Tubes of 20 g. Authorization holderBayer (Switzerland) AG, 8045 Zurich. This leaflet was last checked by the drug authority (Ref:) in December 2021. ..
41.34 USD
Dolo-spedifen forte film-coated tablets 400 mg 10 pcs
What is Dolo-Spedifen forte 400 and when is it used? Dolo-Spedifen forte 400 contains the active ingredient ibuprofen in the form of ibuprofen arginate. This has pain-relieving, Care and antipyretic properties. The effect occurs after about 30 minutes and lasts about 6 hours. Dolo-Spedifen forte 400 is suitable for short-term Care, i.e. for a maximum of 3 days Care of: Pain in the area of joints and ligaments; Back pain; Headache; Toothache; Pain during menstrual bleeding; Pain zen after injuries;Fever with flu-like illnesses.When should Dolo-Spedifen forte 400 not be taken?If you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other pain or Wellness care for medicines, so-called non-steroidal Care drugs;if you are pregnant or breastfeeding (see also «Can Dolo-Spedifen forte 400 be taken during pregnancy or while breastfeeding?»);if you have active stomach and/or duodenal ulcers or gastrointestinal bleeding;if you have a history of gastrointestinal bleeding or perforation (perforation) in connection with previous therapy with so-called non-steroidal Care drugs;if you have chronic intestinal inflammation (Crohn's disease, ulcerative colitis);in the case of cerebral hemorrhage;in the case of an increased tendency to bleed;in the case of severe impairment of liver or kidney function;in the case of severe heart failure;for the Care of pain after a coronary bypass operation on the heart (or use of a heart-lung machine);in children under 12 years of age. Dolo-Spedifen forte 400 has not been tested for use in children under the age of 12. When is caution required when taking Dolo-Spedifen forte 400? During Care with Dolo-Spedifen forte 400, mucosal ulcers in the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) may occur. These complications can occur at any time during Care, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine.Older people may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately.You may only take Dolo-Spedifen forte 400 with a Ref: and under medical supervision in the following situations:if you are currently being treated by a doctor for a serious illness;if you have previously suffered from a stomach or duodenal ulcer;if you have already had a heart attack, stroke or a have had venous thrombosis, or if you have risk factors (such as high blood pressure, diabetes, high levels of fat in your blood, smoking); for certain Cares with a similar effect, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found at high doses and/or long-term Care. It is not known whether this increased risk also applies to Dolo-Spedifen forte 400;if you have heart disease or kidney disease, if you are taking medicines for high blood pressure (e.g. diuretics, ACE inhibitors) or in the event of increased fluid loss, e.g. through heavy sweating; theTaking Dolo-Spedife forte 400 can impair the function of your kidneys, which can lead to an increase in blood pressure and/or fluid retention (oedema);if you have liver problems;if you are being treated with medicines that inhibit blood clotting (blood thinners, anticoagulants) or have a blood clotting disorder;if you suffer from Wellness care for;if you are taking medicines for Care of diabetes, medicines to increase urine output (water tablets), medicines to treat infections (quinolone antibiotics), for AIDS (zidovudine), immunosuppressants (tacrolimus, cyclosporine), corticosteroids, antiplatelet medicines such as acetylsalicylic acid, selective serotonin reuptake inhibitors (SSRIs), antifungal medicines (voriconazole, fluconazole), or medicines containing any of the following: lithium, digoxin, are taking methotrexate, mifepristone, baclofen, phenytoin, probenecid or sulfinpyrazone;if you have certain skin diseases (systemic lupus erythematosus (SLE) or mixed collagenosis);if you have an infection. Dolo-Spedifen forte 400 can mask signs of infection such as fever and pain. It is therefore possible that Dolo-Spedifen forte 400 may delay adequate Care of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately.Serious skin reactions such as acute generalized pustular exanthema, scaly skin inflammation or Stevens-Johnson syndrome have been reported in connection with Care with medicines containing ibuprofen. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, lesions on the mucous membranes, blisters or other signs of allergy, you should stop taking Dolo-Spedifen forte 400 and seek immediate medical attention, as these may be the first signs of a very serious skin reaction (see «What side effects can Dolo-Spedifen forte 400 have?»).Acetylsalicylic acid, other Cares or Cox-2 inhibitors should not be taken at the same time as ibuprofen as the risk of side effects may be increased.Patients who experience visual disturbances during Dolo-Spedifen forte 400 therapy should discontinue Care and consult a doctor immediately.Excipients of particular interestDolo-Spedifen forte 400 film-coated tablets contain:Sucrose: Please take Do not use this medicine until you have consulted your doctor if you know that you have an intolerance to sugar.Sodium: 83 mg sodium (main component of cooking/table salt) per 400 mg film-coated tablet. This corresponds to 4% of the recommended maximum daily dietary intake of sodium for an adult.This medicine may impair your ability to react, drive and use tools or machines.Inform your doctor, Ref: or druggist if you suffer from any other illnesses, have allergies or are taking or using other medicines (including those you have bought yourself)!May do Thurs lo-Spedifen forte 400 taken during pregnancy or while breastfeeding?PregnancyIf you are pregnant or planning a pregnancy, you should only take Dolo-Spedifen forte 400 after consulting your doctor. In the last third of pregnancyDolo-Spedifen forte 400 must not be taken afterwards.BreastfeedingDolo-Spedifen forte 400 should not be taken while breastfeeding unless your doctor has expressly permitted it.How do you use Dolo-Spedifen forte 400?Adults and adolescents from the age of 12D olo-Spedifen forte 400: Take 1 film-coated tablet with plenty of liquid. Before taking the next dose, wait 4 to 6 hours. In the case of pain during menstrual bleeding, it is recommended to start Care with 1 film-coated tablet of Dolo-Spedifen forte 400 at the first sign of symptoms.Maximum daily dose Do not take more than 3 film-coated tablets of Dolo- Spedifen forte 400 within 24 hours, unless prescribed by a doctor.Do not use Dolo-Spedifen forte 400 for more than 3 days and only to treat the symptoms listed above.The lowest effective dose should be used for the shortest time necessary to relieve symptoms.If the symptoms increase despite taking Dolo-Spedifen forte 400 or if the pain is painful en area becomes red or swollen, consult your doctor. A serious illness can be the cause.Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. If you have an infection, consult a doctor immediately if the symptoms (e.g. fever and pain) persist or worsen (see «When should you be careful when taking Dolo-Spedifen forte 400?»).If you have taken more Dolo-Spedifen forte 400 than you should, or if children have accidentally taken the medicine, always consult a doctor to get an assessment of the risk and advice on further Care.Symptoms may include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported.Children under the age of 12Dolo-Spedifen forte 400 must not be used in children under the age of 12. The use and safety of Dolo-Spedifen forte 400 in children under the age of 12 has not yet been systematically tested. Stick to the dosage given in the package insert or prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist.What side effects can Dolo-Spedifen forte 400 have?The following side effects can occur when taking Dolo-Spedifen forte 400, which may require medical Care.Please tell your doctor or your doctor immediately if you experience one or more of the following symptoms and stop taking Dolo-Spedifen forte 400:Very common side effects, which may occur in more than 1 in 10 casesStomach and intestine problems such as indigestion, Wellness care forCommon side effects, which occur in more than 1 in 100 cases but less than 1 in 10 casesGastro-intestinal complaints such as nausea, feeling of fullness, heartburn, pain in the upper abdomen, anorexia, Wellness care for, flatulence, vomiting, erosive inflammation of the gastric mucosa, blood stoolCentral nervous side effects wie Impaired reactions (especially when combined with alcohol), drowsiness, headache and dizzinessDepression, anxiety, confusionVisual disturbances (the visual disturbances are usually reversible if Care is stopped)Ringing in the ears, hearing lossAcute skin rashOccasional side effects, occurring in more than 1 in 1,000 cases but less than 1 in 100 casesAllergic reactions, swelling of the faceWellness care for, spasm of the muscles of the airways and shortness of breathStomach ulcer, gastrointestinal bleeding, tarry stools, gastritisRare side effects, occurring in more than 1 in 10,000 cases but less than 1 in 1,000 casesChanges in the blood countSymptoms of lupus erythematosus (butterfly plexus), aseptic meningitis (meningitis) in patients suffering from an autoimmune disease"Tingling" of the skinIrreversible visual disturbance or visual impairmentPatients with heart failure are at risk of acute pulmonary edema (water lung)Perforation in the stomach and intestines, vomiting blood, ulcers in the oral mucosa, worsening of colitis or Crohn's diseaseLiver failure, liver dysfunctionBlood in the urineVarious kidney diseases such as kidney toxicity, kidney dysfunction with fluid retention in the tissueVery rare side effects occurring in less than 1 in 10'00 0 casesPsychotic statesSevere allergic skin reactions with formation of blisters and/or extensive detachment of the skin, photosensitivity reactions, worsening of skin reactionsAcute kidney failureSide effects with unknown frequency:Wellness care forAnaphyl acute shockHeart failureArterial thrombosis, blood pressure disordersThroat irritationHepatitis, jaundice, liver injuryGeneral swellingSevere skin reaction: Known as DRESS syndrome. Symptoms of DRESS include a rash, fever, swollen lymph nodes and an increase in eosinophils (a type of white blood cell). Known as acute generalized pustular exanthema (AGEP); at the start of Care there is a red, scaly, widespread rash with bumps under the skin and blisters accompanied by fever, primarily on the skin folds, trunk and upper extremities. Discontinue use of Dolo-Spedifen forte 400 if you develop these symptoms and seek medical Care immediately (see also «When should you be careful when taking Dolo-Spedifen forte 400?»).If you notice any side effects, contact your doctor, Ref: or druggist. This also applies in particular to side effects that are not listed in this leaflet.What else needs to be taken into account?The medicine may only be used up to the date marked «EXP» on the container.Storage instructionsStore at room temperature (15–25 °C) and out of the reach of children.Further informationYour doctor or Ref: can provide you with further information or druggist or your doctor, Ref: or druggist. These people have the executiveHonest professional information. What does Dolo-Spedifen forte 400 contain? Active ingredients 1 film-coated tablet contains 400 mg ibuprofen as ibuprofen arginate. Excipients Arginine, sodium bicarbonate, crospovidone, magnesium stearate, film coating: hypromellose, sucrose, titanium dioxide (E1 71), Macrogol 4000.Authorization number56720 (Ref:).Where can you get Dolo-Spedifen forte 400? Which packs are available? in pharmacies and drugstores, without medical Ref:. packs of 10 film -coated tablets for 400 mg. registration owner Zambon Switzerland AG 6814 Cadempino This package insert was last in August 2020 checked (Ref:). ..
31.38 USD
Ecofenac sandoz lipogel 1% tube 50g
Ecofenac Sandoz Lipogel 1% Tb 50 g Ecofenac Sandoz Lipogel 1% Tb 50 g is an effective topical Care medicine for the Care of mild to moderate pain and inflammation. It is a non-steroidal Care drug (NSAID) and contains the active ingredient diclofenac diethylammonium. The gel is specially formulated in a lipophilic base that allows for easy and deep penetration into the skin, resulting in fast and long-lasting Care. It absorbs quickly into the skin without leaving any grease or residue, making it convenient for use during the day and at night. Ecofenac Sandoz Lipogel 1% Tb 50 g is suitable for the Care of conditions such as Wellness care for, back pain, sprains, strains, and sports injuries. It provides targeted Care by reducing the production of prostaglandins, which are responsible for causing inflammation and pain in the affected area. The product comes in a convenient 50g tube, making it easy to carry and apply on-the-go. It is recommended to apply the gel to the affected area two to three times daily, gently massaging it into the skin until fully absorbed. Ecofenac Sandoz Lipogel 1% Tb 50 g is a safe and effective alternative to oral pain medications, as it works locally without affecting the rest of the body. However, it is still important to follow the recommended dosage and not exceed the maximum daily dose of 150 mg. If you are pregnant, breastfeeding, or have a history of stomach ulcers or hypersensitivity to NSAIDs, it is recommended to consult a healthcare provider before using this product. ..
15.81 USD
Elixan eucalyptus 80/85 oil 10 ml
Elixan Eucalyptus 80/85 Oil 10 ml is a premium quality product from the renowned brand Elixan. This oil is distilled from the leaves of the Eucalyptus tree, offering a concentrated essence that is rich in therapeutic properties. Our Elixan Eucalyptus Oil is characterized by its 80/85 eucalyptol content. This high concentration of eucalyptol ensures a potent and effective solution for various applications. Its refreshing and clean scent makes it a popular choice for aromatherapy, promoting a sense of calm and relaxation. Key Features: High-Quality Eucalyptus Oil: Distilled from the leaves of the Eucalyptus tree, ensuring a pure and natural product. High Eucalyptol Content: With an 80/85 eucalyptol concentration, our oil offers superior effectiveness. Relaxing Aroma: The clean, refreshing scent of Eucalyptus is ideal for promoting a sense of calm and relaxation. 10 ml Bottle: Conveniently packaged in a 10 ml bottle for easy use and storage. Benefits: Therapeutic Properties: Eucalyptus oil is known for its healing properties, helping to soothe muscle pain and reduce inflammation. Aromatherapy: The refreshing scent of Eucalyptus can help to reduce stress and anxiety, promoting a sense of calm and relaxation. Home Use: Eucalyptus oil is a natural and effective solution for cleaning and disinfecting surfaces in your home. Use Cases: Wellness and Wellness: Add a few drops to a diffuser for a relaxing aromatherapy session, or mix with a carrier oil for a soothing massage. Home Cleaning: Mix with water and use as a natural disinfectant for cleaning surfaces in your home. Personal Care: Incorporate into your skincare routine for its antimicrobial and Care properties. Experience the therapeutic benefits of the Elixan Eucalyptus 80/85 Oil 10 ml and discover a natural solution for your health, wellness, and home needs...
21.00 USD
Gelodurat caps 120 pcs
What GeloDurat is and what it is used forGeloDurat contains 300 mg distillate of essential oils from various plants and is used for acute and chronic Wellness care for and inflammation of the paranasal sinuses (acute and chronic sinusitis).GeloDurat liquefies the mucus in the bronchi and paranasal sinuses, promotes the removal of this mucus and makes it easier to expectorate.GeloDurat reduces the aggravation of the disease that is common in chronic courses.What precautions should be taken?Support the expectorant effect of GeloDurat by drinking a lot.When should GeloDurat not be taken or only with caution?GeloDurat should not be taken in case of hypersensitivity to any of the components of the drug.Do not use on children under 4 years of age.Inform your doctor, Ref: or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!).Can GeloDurat be taken during pregnancy or while breastfeeding?Based on the results of animal experiments and many years of therapeutic experience in humans, it can be assumed according to the current state of scientific knowledge that GeloDurat can also be taken during pregnancy without risk after consultation with the doctor treating you.GeloDurat is considered to be very likely to pass into breast milk. For this reason, GeloDurat should only be used during breastfeeding after consulting a doctor.How do you use GeloDurat?For acute, inflammatory symptoms, adults take 1 capsule 3-4 times a day, children over 10 years of age take 1 capsule 1-3 times a day. In the case of chronic diseases, take one capsule twice a day. This dosage is also recommended for long-term Care.GeloDurat capsules should be swallowed whole with plenty of cold liquid half an hour before eating.Use on children under 10 years of age only if prescribed by a doctor. Do not use on children under 4 years of age.To make it easier to cough up in the morning if you have chronic Wellness care for, you can take an additional GeloDurat capsule in the evening before you go to bed.To facilitate a night's rest, the last dose can be taken before bedtime.In the case of respiratory diseases that last longer than 7 days, a doctor, Ref: or druggist must be consulted.Follow the dosage given in the package leaflet or prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist.What side effects can GeloDurat have?The following side effects may occur when taking GeloDurat:GeloDurat can cause gastrointestinal symptoms such as stomach or abdominal pain, vomiting, nausea, Wellness care for and flatulence. If kidney and gallstones are present, they can be set in motion.In individual cases, the occurrence of hypersensitivity reactions (e.g. skin rash, swelling of the face, shortness of breath or circulatory disorders) has been reported.If you notice any side effects that are not described here, you should inform your doctor, Ref: or druggist.What should also be noted?Do not store GeloDurat above 25 °C. Store in the original packaging and outer carton.The Care product may only be used up to the date marked “EXP” on the package.Your doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists.What does GeloDurat contain?1 enteric-coated capsule contains 300 mg distillate of essential oils of eucalyptus and myrtle leaves, sweet orange and lemon peel.This preparation also contains auxiliary substances.Registration Number55928 (Ref:)Where can you get GeloDurat? What packs are available?In pharmacies and drugstores, without medical Ref:.Packs of 30, 60 and 120 capsules.Marketing Authorization HolderGebro Pharma AG, CH-4410 LiestalManufacturerG. Pohl-Boskamp GmbH & Co. KG, D-25551 Hohenlockstedt...
129.02 USD
Ibu sandoz film-coated tablets 400 mg 10 pcs
Ibu Sandoz contains the active ingredient ibuprofen. It has pain-relieving, fever-reducing and Care properties. Ibu Sandoz is suitable for short-term Care, i. for a maximum of 3 days Care of: Pain in the area of joints and ligaments; Back pain; Headache; Toothache; Pain during of menstrual bleeding; Pain after injury; Fever with flu-like illnesses. Ref:-approved patient information Ibu Sandoz® 400Sandoz Vitals AGWhat is Ibu Sandoz and when is it used ? Ibu Sandoz contains the active ingredient ibuprofen. It has pain-relieving, fever-reducing and Care properties. Ibu Sandoz is suitable for short-term Care, i. for a maximum of 3 days Care of: Pain in the area of joints and ligaments;Back pain;Headache;Toothache;Pain during of the menstrual period;Pain after injuries;Fever with flu-like illnesses.When can Ibu Sandoz not to be taken? Ibu Sandoz must not be taken, if you are allergic to any of the ingredients or have had shortness of breath or allergy-like skin reactions after taking acetylsalicylic acid or other Cares or Wellness care for medicines called non-steroidal Care drugs,if you are pregnant are or are breastfeeding (see also the chapter "Can Ibu Sandoz be taken while pregnant or breastfeeding?"),if you suffer from a stomach and/or duodenal ulcer or gastrointestinal bleeding,in chronic intestinal inflammation (Crohn's disease, ulcerative colitis),in severe impairment of liver or kidney function,in severe heart failure,for the Care of pain after coronary heart bypass surgery (or use of a heart-lung machine),in children under 12 years of age. Ibu Sandoz has not been tested for use in children under the age of 12.When should you be careful when taking Ibu Sandoz? During Care with Ibu Sandoz, ulcers in the mucous membranes of the upper gastrointestinal tract, rarely bleeding or, in isolated cases, perforations (perforations in the stomach or intestines) may occur. These complications can occur at any time during Care, even without warning symptoms. To reduce this risk, the smallest effective dose should be used over the shortest possible duration of therapy. Contact your doctor if you have stomach pain and suspect it is related to taking the medicine or if you have an infection - see below under 'Infection'. For certain Cares, the so-called COX-2 inhibitors, an increased risk of heart attack and stroke has been found at high doses and/or long-term Care. This risk can also be slightly increased with Ibu Sandoz at a high dose (2400 mg/day). However, at the usual dosage (maximum 1200 mg/day), no increase in this risk was found. If you have already had a heart attack, stroke or venous thrombosis, the use of high doses of Ibu Sandoz is no longer recommended. Do not exceed the recommended dose or duration of Care and always tell your doctor if you have had a heart attack, stroke or thrombosis in a vein, or if you have risk factors (such as high blood pressure, diabetes (sugar diabetes), high blood fat levels, Smoking. Your doctor will decide if you can still use Ibu Sandoz and what dose is right for you.Taking Ibu Sandoz can affect the way your kidneys work, which can lead to an increase in blood pressure and/or fluid retention (oedema). Tell your doctor if you have heart or kidney disease, if you are taking medicines to treat high blood pressure (e.g. diuretics, ACE inhibitors) or if you lose more fluids, e.g. through heavy sweating. This medicine may impair your ability to react, the ability to drive and the ability to use tools or machines! This is especially true when taken with alcohol. Caution is indicated in patients with a history of gastric or duodenal ulcers, impaired liver, kidney or heart function, blood clotting disorders, and in patients suffering from Wellness care for, chronic inflammation of the nasal mucosa (chronic runny nose), allergic diseases or certain rheumatic diseases (lupus erythematosus or collagen diseases). Serious skin reactions have been reported in association with medicines containing ibuprofen. You should stop taking Ibu Sandoz and see a doctor straight away if you develop a rash, mucosal lesions, blisters or any other sign of allergy, as these can be the first signs of a very serious skin reaction. The highest risk of such reactions appears to be at the beginning of therapy. If you develop a skin rash, lesions on the mucous membranes, blisters or any other sign of allergy, you should stop taking Ibu Sandoz and seek medical attention immediately, as these may be the first signs of a very serious skin reaction (see the section «What side effects can Ibu Sandoz have? »). Ibu Sandoz should not be used if you have chickenpox. InfectionsIbu Sandoz may mask signs of infections such as fever and pain. It is therefore possible that Ibu Sandoz may delay adequate Care of the infection, which may lead to an increased risk of complications. This has been seen in bacterial pneumonia and bacterial skin infections associated with chickenpox. If you are taking this medicine during an infection and your infection symptoms persist or worsen, consult a doctor immediately. Tell your doctor, Ref: or druggist if you have recently been treated for an abortion. Tell your doctor, Ref: or druggist if you are being treated with medicines such as blood thinners (e.g. low-dose acetylsalicylic acid), diuretics (water tablets), ACE inhibitors or β-blockers (preparations for high blood pressure). and heart failure), antibiotics, certain antifungal medicines (e.g. voriconazole or fluconazole), immunosuppressants (preparations against transplant rejection), Ginkgo biloba plant extract, medicines for high blood sugar, AIDS, epilepsy and depression. Nonsteroidal Care drugs such as ibuprofen and the medicines listed above can interact. In particular, long-term Care with Ibu Sandoz may reduce the cardioprotective effect of low-dose acetylsalicylic acid. Acetylsalicylic acid or other pain relievers should not be taken at the same time as ibuprofen as the risk of side effects may be increased. Side effects, particularly those affecting the gastrointestinal tract or the central nervous system, can be increased if alcohol is consumed at the same time. Prolonged use of Cares can cause headaches. Do not treat them with an increased dose of the drug, but inform your doctor. Elderly patientsElderly patients are more likely to experience side effects after using non-steroidal Care drugs, especially bleeding and perforation in the stomach and intestines. Therefore, particularly careful medical supervision is required in elderly patients. This Care product contains less than 1 mmol sodium (23 mg) per film-coated tablet, i.e. essentially 'sodium-free'. it is almost «sodium-free». Tell your doctor, Ref: or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally.Can Ibu Sandoz be taken during pregnancy or breastfeeding?PregnancyIf you are pregnant or planning to become pregnant, you should only take Ibu Sandoz after consulting your doctor. Ibu Sandoz should not be taken during the last trimester of pregnancy. BreastfeedingIbu Sandoz should not be taken while breastfeeding unless your doctor has given you permission to do so. How do you use Ibu Sandoz?Adults and adolescents aged 12 and over Take 1 film-coated tablet Ibu Sandoz with plenty of liquid. The film-coated tablets can be swallowed whole or divided to halve the dose or for ease of administration. A gap of 6 to 8 hours should be observed before the next dose. Maximum daily doseDo not take more than 3 film-coated tablets of Ibu Sandoz in a 24-hour period, unless prescribed by a doctor. In the case of pain during the menstrual period, it is recommended to start Care at the first sign of the symptoms. Do not use Ibu Sandoz for more than 3 days and only to treat the conditions listed above. If symptoms worsen despite taking Ibu Sandoz, or if the painful area becomes red or swollen, consult your doctor. A serious illness can be the cause. Even if the symptoms do not improve within 3 days at the latest, you should consult your doctor so that the reason can be clarified. Children under 12 yearsIbu Sandoz should not be used in children under 12 years of age. The use and safety of Ibu Sandoz in children under the age of 12 has not been systematically evaluated. Elderly patientsElderly patients may be more sensitive to the medicine than younger adults. It is particularly important that elderly patients report any side effects to their doctor immediately. If you have taken more Ibu Sandoz than you should, always consult a doctor for an assessment of the risk and advice on further Care. Symptoms can include nausea, stomach pain, vomiting (possibly with blood), headache, ringing in the ears, confusion and eye tremors. At high doses, drowsiness, chest pain, palpitations, fainting, convulsions (especially in children), weakness and dizziness, blood in the urine, feeling cold and breathing problems have been reported. If you forget to take a dose, do not take more than the usual recommended amount next time. Stick to the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Ibu Sandoz have?The following side effects can occur when taking Ibu Sandoz. They are listed by frequency: Common (affects 1 to 10 users in 100)gastrointestinal disorders such as indigestion, Wellness care for, nausea, vomiting, Wellness care for, upper abdominal pain, Flatulence, tarry stool, vomiting blood, gastrointestinal bleeding.Central nervous side effects such as restricted reaction time (especially in combination with alcohol), headache and dizziness.Acute skin rash. Uncommon (affects 1 to 10 users in 1000)Inflammation of the nasal mucosa.Hypersensitivity reactions...
21.99 USD
Ichtholan ointment 10% tube 40 g
Ichtholan Zugsalbe contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, Care and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseases ICHTHOLAN 20% ointment for deeper inflammatory skin diseases, such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands. ICHTHOLAN 50% Ointment for the maturation of boils Ref:-approved patient information ICHTHOLAN® 10%, 20%, 50% traction ointmentMerz Pharma (Switzerland) AGWhat is Ichtholan 10%, 20%, 50% traction ointment and when is it used? Ichtholan traction ointment contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, Care and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseasesICHTHOLAN 20% ointment for deeper inflammatory skin diseases such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands.ICHTHOLAN 50% Pulling ointment for the maturation of boilsWhen may Ichtholan 10 %, 20%, 50% traction ointment not to be used? Known hypersensitivity to Ichthammolum (ammonium bituminosulfonate), or one of the excipients according to the composition. The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. When is caution required when using Ichtholan 10%, 20%, 50% traction ointment?In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation is passed on by smear infection and eventually a hard-to-control furunculosis (the recurrence of boils) develops. Careful bandaging technique is therefore necessary (see «How do you use Ichtholan Zugsalbe?»). If a local deterioration occurs or if there is no healing within 2-3 weeks, a doctor or Ref: should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. During Care with Ichtholan traction ointment in the genital and anal area, the fats and emulsifiers contained as auxiliary substances and the simultaneous use of latex condoms can lead to a reduction in the tear strength and thus to an impairment of the safety of the condoms. The use of other ointments or creams can impair the effect of Ichtholan Zugsalbe. Ichtholan can increase the solubility of other active ingredients and thus enhance their absorption into the skin. Ichtholan contains butylated hydroxytoluene and wool wax, which can cause localized skin reactions (e.g. contact dermatitis). Butylated hydroxytoluene can also cause irritation to the eyes and mucous membranes. Tell your doctor, Ref: or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Ichtholan 10%, 20%, 50% traction ointment be used during pregnancy or breastfeeding?PregnancyThere are insufficient data for the use of Ichtholan Zugsalbe during pregnancy. If you are pregnant or would like to become pregnant, only use Ichtholan Zugsalbe on the Ref: of your doctor. A large area application during pregnancy will Generally discouraged. BreastfeedingIt is not known whether the active ingredient in Ichtholan is excreted in human milk. Breastfeeding women should only use Ichtholan Zugsalbe if prescribed by their doctor. Ichtholan traction ointment should not be used on the breasts while breastfeeding. How do you use Ichtholan 10%, 20%, 50% Draw Balm?Ichtholan 10% Draw BalmIf unless otherwise prescribed by the doctor, Ichtholan 10% Zugsalbe is applied thinly to the inflamed skin regions once a day and distributed well. The Care can be carried out until the inflammation of the skin has subsided. Ichtholan 20% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 20% traction ointment is applied thickly to the skin regions to be treated and covered over a large area with a bandage . For this purpose, a cotton swab can be placed on the applied ointment, for example, and this can be covered over a large area with a plaster. The dressing is changed daily. Every time the bandage is changed, the ointment residues on the skin must be washed off with warm water and soap before you start treating again with Ichtholan 20% Zugointment. The duration of Care depends on the response. ICHTHOLAN 50% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 50% traction ointment is applied to the skin region to be treated as thick as a knife back and covered over a large area with a bandage . The bandage should be changed after 3 days at the latest. The duration of use depends on the success of the Care. Whenever the bandage is changed, the ointment residue should be washed off with lukewarm water and soap before treating again with 50% Zugointment. In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation will be passed on by smear infection and furunculosis (the repeated occurrence of boils) may develop that is difficult to influence. Therefore, a careful bandaging technique is necessary: Meticulous cleanliness, cleaning and disinfection of the surrounding healthy skinPut on a well-covering, non-slipping and non-abrasive bandagePossibly bathing with disinfectant additives.The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. Stick to the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Ichtholan 10%, 20%, 50% Zugointment have?The following side effects can occur when using Ichtholan Zugointment: Rarely (affects 1 to 10 users in 10,000)Intolerance reactions of the skin that manifest themselves as itching, burning or reddening of the skin; allergic skin reactions (contact dermatitis). Very rare (affects less than 1 in 10,000 people)severe skin reactions, e.g. blistering (under an airtight bandage). If these symptoms occur, a doctor should be consulted. If you get any side effects, talk to your doctor, Ref: or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The Care product may only be used up to the date marked «EXP» on the container. Tubes should be closed well after opening. Any ointment stains can be easily removed from the laundry by first using an organic solvent (e.g. petrol) and then washing with a detergent. Storage instructionsMedicines should be kept out of the reach of children. Store at room temperature (15-25 °C) and dry. Your doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does Ichtholan 10%, 20%, 50% Zugsalve contain?Active ingredients10% and 20%: 1 g ointment contains: Ichthammolum (ammonium bituminosulfonate) 100 mg/200 mg. 50%: 1 g of ointment contains: Ichthammolum (ammonium bituminosulfonate) 500 mg. Excipients10%: wool wax, butylated hydroxytoluene (E321), yellow vaseline, purified water. 20%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, purified water. 50%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, microcrystalline wax, purified water. Approval number10751 (Ref:) Where can you get Ichtholan 10%, 20%, 50% Zugsalve? What packs are available?In pharmacies and drugstores, without a doctor's Ref:. Tubes of 40g ointment. Authorization holderMerz Pharma (Switzerland) AG, 4123 Allschwil ManufacturerIchthyol-Gesellschaft Cordes, Hermanni & Co. (GmbH & Co.) KG, Hamburg, Germany This leaflet was last checked by the drug authority (Ref:) in April 2019. ..
68.70 USD
Ichtholan ointment 20% tube 40 g
Ichtholan Zugsalbe contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, Care and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseases ICHTHOLAN 20% ointment for deeper inflammatory skin diseases, such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands. ICHTHOLAN 50% Ointment for the maturation of boils Ref:-approved patient information ICHTHOLAN® 10%, 20%, 50% traction ointmentMerz Pharma (Switzerland) AGWhat is Ichtholan 10%, 20%, 50% traction ointment and when is it used? Ichtholan traction ointment contains Ichthammolum (ammonium bituminosulfonate) as an active ingredient and has an antibacterial, Care and antipruritic effect. In purulent skin processes, in the advanced stage of the inflammation, it accelerates the melting of the focus of the disease and the breakthrough of the pus to the outside. Ichtholan Zugsalbe is used in different concentrations to treat various inflammatory diseases of the skin: ICHTHOLAN 10% ointment for superficial inflammatory skin diseasesICHTHOLAN 20% ointment for deeper inflammatory skin diseases such as abscesses, Inflammation of the nail bed, inflammation of the sweat glands and abscesses of the sweat glands.ICHTHOLAN 50% Pulling ointment for the maturation of boilsWhen may Ichtholan 10 %, 20%, 50% traction ointment not to be used? Known hypersensitivity to Ichthammolum (ammonium bituminosulfonate), or one of the excipients according to the composition. The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. When is caution required when using Ichtholan 10%, 20%, 50% traction ointment?In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation is passed on by smear infection and eventually a hard-to-control furunculosis (the recurrence of boils) develops. Careful bandaging technique is therefore necessary (see «How do you use Ichtholan Zugsalbe?»). If a local deterioration occurs or if there is no healing within 2-3 weeks, a doctor or Ref: should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. During Care with Ichtholan traction ointment in the genital and anal area, the fats and emulsifiers contained as auxiliary substances and the simultaneous use of latex condoms can lead to a reduction in the tear strength and thus to an impairment of the safety of the condoms. The use of other ointments or creams can impair the effect of Ichtholan Zugsalbe. Ichtholan can increase the solubility of other active ingredients and thus enhance their absorption into the skin. Ichtholan contains butylated hydroxytoluene and wool wax, which can cause localized skin reactions (e.g. contact dermatitis). Butylated hydroxytoluene can also cause irritation to the eyes and mucous membranes. Tell your doctor, Ref: or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Ichtholan 10%, 20%, 50% traction ointment be used during pregnancy or breastfeeding?PregnancyThere are insufficient data for the use of Ichtholan Zugsalbe during pregnancy. If you are pregnant or would like to become pregnant, only use Ichtholan Zugsalbe on the Ref: of your doctor. A large area application during pregnancy will Generally discouraged. BreastfeedingIt is not known whether the active ingredient in Ichtholan is excreted in human milk. Breastfeeding women should only use Ichtholan Zugsalbe if prescribed by their doctor. Ichtholan traction ointment should not be used on the breasts while breastfeeding. How do you use Ichtholan 10%, 20%, 50% Draw Balm?Ichtholan 10% Draw BalmIf unless otherwise prescribed by the doctor, Ichtholan 10% Zugsalbe is applied thinly to the inflamed skin regions once a day and distributed well. The Care can be carried out until the inflammation of the skin has subsided. Ichtholan 20% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 20% traction ointment is applied thickly to the skin regions to be treated and covered over a large area with a bandage . For this purpose, a cotton swab can be placed on the applied ointment, for example, and this can be covered over a large area with a plaster. The dressing is changed daily. Every time the bandage is changed, the ointment residues on the skin must be washed off with warm water and soap before you start treating again with Ichtholan 20% Zugointment. The duration of Care depends on the response. ICHTHOLAN 50% traction ointmentUnless otherwise prescribed by the doctor, Ichtholan 50% traction ointment is applied to the skin region to be treated as thick as a knife back and covered over a large area with a bandage . The bandage should be changed after 3 days at the latest. The duration of use depends on the success of the Care. Whenever the bandage is changed, the ointment residue should be washed off with lukewarm water and soap before treating again with 50% Zugointment. In the case of purulent skin inflammation, especially boils, there is a risk that the inflammation will be passed on by smear infection and furunculosis (the repeated occurrence of boils) may develop that is difficult to influence. Therefore, a careful bandaging technique is necessary: Meticulous cleanliness, cleaning and disinfection of the surrounding healthy skinPut on a well-covering, non-slipping and non-abrasive bandagePossibly bathing with disinfectant additives.The use and safety of Ichtholan Zugsalbe in children under the age of 12 has not yet been tested. Stick to the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Ichtholan 10%, 20%, 50% Zugointment have?The following side effects can occur when using Ichtholan Zugointment: Rarely (affects 1 to 10 users in 10,000)Intolerance reactions of the skin that manifest themselves as itching, burning or reddening of the skin; allergic skin reactions (contact dermatitis). Very rare (affects less than 1 in 10,000 people)severe skin reactions, e.g. blistering (under an airtight bandage). If these symptoms occur, a doctor should be consulted. If you get any side effects, talk to your doctor, Ref: or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The Care product may only be used up to the date marked «EXP» on the container. Tubes should be closed well after opening. Any ointment stains can be easily removed from the laundry by first using an organic solvent (e.g. petrol) and then washing with a detergent. Storage instructionsMedicines should be kept out of the reach of children. Store at room temperature (15-25 °C) and dry. Your doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does Ichtholan 10%, 20%, 50% Zugsalve contain?Active ingredients10% and 20%: 1 g ointment contains: Ichthammolum (ammonium bituminosulfonate) 100 mg/200 mg. 50%: 1 g of ointment contains: Ichthammolum (ammonium bituminosulfonate) 500 mg. Excipients10%: wool wax, butylated hydroxytoluene (E321), yellow vaseline, purified water. 20%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, purified water. 50%: wool wax, butylated hydroxytoluene (E321), yellow petroleum jelly, microcrystalline wax, purified water. Approval number10751 (Ref:) Where can you get Ichtholan 10%, 20%, 50% Zugsalve? What packs are available?In pharmacies and drugstores, without a doctor's Ref:. Tubes of 40g ointment. Authorization holderMerz Pharma (Switzerland) AG, 4123 Allschwil ManufacturerIchthyol-Gesellschaft Cordes, Hermanni & Co. (GmbH & Co.) KG, Hamburg, Germany This leaflet was last checked by the drug authority (Ref:) in April 2019. ..
73.82 USD
Kytta ointment 100 g
Herbal medicineWhat is Kytta ointment and when is it used?Kytta ointment contains an extract made from the fresh roots of Symphytum officinale (common comfrey) using a special process. Kytta ointment has a decongestant, pain-relieving and Care effect. Kytta ointment is non-greasy and non-lubricating and is therefore easy to wash off. Kytta ointment is used externally to support the Care of degenerative-rheumatoid diseases (e.g. knee Wellness care for), muscle, joint and nerve pain, and blunt, bloodless injuries such as bruises, strains and sprains. It is also used for tendonitis and, if the doctor recommends it, for the aftercare of bone fractures and dislocations.When should Kytta ointment not be used or should it only be used with caution?Kytta ointment must not be used in case of known hypersensitivity to any of the ingredients (see composition) or in children under 3 years of age.Do not use if you are prone to allergies. Kytta ointment must not be used on open wounds or mucous membranes. The eye, nose and mouth areas should be excluded from Care with Kytta ointment.Inform your doctor, Ref: or druggist if you suffer from other illnesses, have allergies or are taking or using other medicines externally (including those you have bought yourself)!Can Kytta ointment be used during pregnancy or while breastfeeding?Based on experience to date, there is no known risk to the child when used as directed. However, systematic scientific studies have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding, or ask your doctor, Ref: or druggist for advice.How do you use Kytta ointment?Unless otherwise prescribed by the doctor, apply Kytta ointment thinly up to 5 times a day and massage in carefully. (In severe cases, apply an ointment dressing.) In children between 3 and 12 years of age, the Care period should not exceed one week.Follow the dosage instructions in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist.What side effects can Kytta ointment have?Rarely, allergic local skin reactions (itching of the skin, reddening of the skin, contact dermatitis, Wellness care for, burning of the skin). Very rarely, systemic hypersensitivity reactions, e.g. generalized skin reactions.In such cases, Care should be stopped and a doctor should be consulted.If you notice any side effects not listed here, you should inform your doctor or Ref:.What should also be noted?This medicine should only be used until the date stated on the container with “EXP”.Keep Kytta ointment out of the reach of children. Store at room temperature (15–25 °C). Shelf life after opening: 12 months.Your doctor, Ref: or druggist will be able to provide you with further information.What is contained in Kytta ointment?1 g of ointment contains: 350 mg liquid comfrey extract from fresh roots, drug-extract ratio 1:2, extraction agent: ethanol 52% (m/m). This preparation also contains excipients and flavourings, vanillin, lauryl sulphate, the preservatives E214, E216, E218, butyl/isobutyl parahydroxybenzoate, phenoxyethanol.Registration number20713 (Ref:).Where can you get Kytta ointment? What packages are available?In pharmacies and drugstores, without medical Ref:.Packs of 50 g, 100 g and 150 g.Marketing Authorisation HolderProcter & Gamble International Operations SA, Lancy.Domicile: 1213 Petit-LancyManufacturerP&G Wellness Austria GmbH & Co. OG, Spittal, Austria. ..
85.55 USD
Kytta ointment 50 g
Herbal medicineWhat is Kytta ointment and when is it used?Kytta ointment contains an extract made from the fresh roots of Symphytum officinale (common comfrey) using a special process. Kytta ointment has a decongestant, pain-relieving and Care effect. Kytta ointment is non-greasy and non-lubricating and is therefore easy to wash off. Kytta ointment is used externally to support the Care of degenerative-rheumatoid diseases (e.g. knee Wellness care for), muscle, joint and nerve pain, and blunt, bloodless injuries such as bruises, strains and sprains. It is also used for tendonitis and, if the doctor recommends it, for the aftercare of bone fractures and dislocations.When should Kytta ointment not be used or should it only be used with caution?Kytta ointment must not be used in case of known hypersensitivity to any of the ingredients (see composition) or in children under 3 years of age.Do not use if you are prone to allergies. Kytta ointment must not be used on open wounds or mucous membranes. The eye, nose and mouth areas should be excluded from Care with Kytta ointment.Inform your doctor, Ref: or druggist if you suffer from other illnesses, have allergies or are taking or using other medicines externally (including those you have bought yourself)!Can Kytta ointment be used during pregnancy or while breastfeeding?Based on experience to date, there is no known risk to the child when used as directed. However, systematic scientific studies have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding, or ask your doctor, Ref: or druggist for advice.How do you use Kytta ointment?Unless otherwise prescribed by the doctor, apply Kytta ointment thinly up to 5 times a day and massage in carefully. (In severe cases, apply an ointment dressing.) In children between 3 and 12 years of age, the Care period should not exceed one week.Follow the dosage instructions in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist.What side effects can Kytta ointment have?Rarely, allergic local skin reactions (itching of the skin, reddening of the skin, contact dermatitis, Wellness care for, burning of the skin). Very rarely, systemic hypersensitivity reactions, e.g. generalized skin reactions.In such cases, Care should be stopped and a doctor should be consulted.If you notice any side effects not listed here, you should inform your doctor or Ref:.What should also be noted?This medicine should only be used until the date stated on the container with “EXP”.Keep Kytta ointment out of the reach of children. Store at room temperature (15–25 °C). Shelf life after opening: 12 months.Your doctor, Ref: or druggist will be able to provide you with further information.What is contained in Kytta ointment?1 g of ointment contains: 350 mg liquid comfrey extract from fresh roots, drug-extract ratio 1:2, extraction agent: ethanol 52% (m/m). This preparation also contains excipients and flavourings, vanillin, lauryl sulphate, the preservatives E214, E216, E218, butyl/isobutyl parahydroxybenzoate, phenoxyethanol.Registration number20713 (Ref:).Where can you get Kytta ointment? What packages are available?In pharmacies and drugstores, without medical Ref:.Packs of 50 g, 100 g and 150 g.Marketing Authorisation HolderProcter & Gamble International Operations SA, Lancy.Domicile: 1213 Petit-LancyManufacturerP&G Wellness Austria GmbH & Co. OG, Spittal, Austria. ..
53.74 USD
Naturkraftwerke aloe vera tube gel 120 ml
Naturkraftwerke Aloe Vera Gel 99% 120 ml Naturkraftwerke Aloe Vera Gel is a natural and pure product that is perfect for all skin types. Made with 99% pure Aloe Vera extract, this gel moisturizes and nourishes the skin from within, leaving it soft, supple, and healthy-looking. The Aloe Vera plant is known for its healing properties and has been used for centuries to treat various skin issues such as burns, scars, and dryness. This non-greasy formula gets easily absorbed into the skin and provides instant relief from itching and redness. It soothes and calms irritated skin with its Care and antibacterial properties. Naturkraftwerke Aloe Vera Gel restores the skin's natural balance and helps in reducing fine lines, wrinkles, and pigmentation. This gel is also suitable for sensitive skin types and can be used as a daily moisturizer. Key Features: 99% pure Aloe Vera gel Non-greasy formula Moisturizes and nourishes the skin Relieves itching and redness Restores the skin's natural balance Directions for Use: Apply Naturkraftwerke Aloe Vera Gel onto clean skin and massage gently until it gets absorbed. Use it as a daily moisturizer or whenever required. Store the gel in a cool and dry place, away from direct sunlight. ..
35.11 USD
Nurofen drag 200 mg 20 pcs
Nurofen Drag 200 mg of 20 pcs Nurofen Drag 200 mg of 20 pcs is a fast-acting pain reliever that swiftly alleviates pain and inflammation. The drug comes in tablet form and can be ingested without water. This medication is designed to provide relief for a variety of pain types, including headaches, menstrual cramps, dental pain, muscle pain, and fever. The active ingredient in Nurofen Drag tablets is ibuprofen, which is a non-steroidal Care drug (NSAID) that operates by reducing the production of the called prostaglandin that causes inflammation and pain. The dosage is a 200 mg tablet per dose, with a maximum of four doses per day. The medication is for adults and children aged 12 and up who weigh at least 40 kg. Nurofen Drag 200 mg of 20 pcs is designed to be swiftly absorbed by the body, with effects that last for up to 8 hours. Since the tablet dissolves in the mouth, it enables active time relief during on-the-go activities like school, work, or commuting. The active formula is powerful, effective, and safe when used as directed, making it a reliable choice for Care. In summary, Nurofen Drag 200 mg of 20 pcs is a powerful, fast-acting, swallow-free Care medication that helps alleviate various types of pain, including headaches, menstrual cramps, dental pain, muscle pain, and fever. With a time-tested, active ingredient, Ibuprofen, and a tablet form that dissolves in the mouth, this medication provides swift Care for adults and children aged 12 and up who weigh at least 40 kg. ..
32.72 USD
Repair gel 100g
Reparil N Gel is an alcoholic drug with a decongestant, Care and analgesic effect. The active ingredient aescin reduces accumulations of water in the tissue and causes the tissue to decongest. The salicylic acid compound has analgesic and Care effects. Reparil N Gel is suitable for the local Care of inflammation, pain, bruising and swelling, e.g. as a result of sprains, bruises and strains. Ref:-approved patient informationReparil® N GelMEDA Pharma GmbHWhat is Reparil N Gel and when is it used?Reparil N Gel is an alcohol-based drug with a decongestant, Care and analgesic effect. The active ingredient aescin reduces accumulations of water in the tissue and causes the tissue to decongest. The salicylic acid compound has analgesic and Care effects. Reparil N Gel is suitable for the local Care of inflammation, pain, bruising and swelling, e.g. as a result of sprains, bruises and strains. When must Reparil N Gel not be used?Reparil N Gel must not be used In the event of hypersensitivity to one of the active ingredients or excipients or in the event of hypersensitivity to other pain-relieving and Care substances, in particular acetylsalicylic acid/aspirin,open injuries, inflammation or infections of the skin and Wellness care for or on mucous membranes and on radiation-treated skin areas,in infants and small children under the age of 2 years.When is Reparil N Gel used Caution required?Reparil N Gel should not be applied to open areas of skin. Avoid contact with eyes. Before applying a bandage, Reparil N Gel should dry on the skin for a few minutes. The use of an occlusive dressing is not recommended. Special care is required when using Reparil N Gelif you suffer from Wellness care for, hay fever, swelling of the nasal mucosa (so-called nasal polyps) or chronic obstructive pulmonary diseases or chronic respiratory infections (especially combined with hay fever-like symptoms)if you are hypersensitive (allergic) to pain and and Wellness care for drugs of all kinds, you are more at risk of Wellness care for attacks (analgesic intolerance/analgesic Wellness care for), local swelling of the skin and mucous membranes (Quincke's edema) or urticaria than other patients;if you are taking other substances hypersensitive (allergic) reactions, e.g. with skin reactions, itching or hives;in acute conditions that are accompanied by severe redness, swelling or overheating of the joints, in the case of persistent or worsening symptoms. In this case, you should consult a doctor.Veneitis caused by a blood clot (thrombosis) should not be massaged. Reparil N Gel should not be used on large areas over a long period of time, unless prescribed by a doctor. Since the salicylic acid compound contained in the drug penetrates the skin to a considerable extent and can lead to undesirable effects, caution is advised in patients with kidney dysfunction and in children. Long-term Care over large areas should be avoided in such patients. Furthermore, it cannot be ruled out that if the gel is applied to large areas and if blood-thinning medication or medication to treat high blood sugar is taken at the same time, their effect will be increased. The undesirable effects of methotrexate can be increased. Inform your doctor, Ref: or druggist if you have used similar products in the past and these led to allergic reactions and if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Reparil N Gel be used during pregnancy or breastfeeding?Reparil N Gel must not be used during pregnancy and breastfeeding unless expressly prescribed by a doctor. Then it should only be used for a short time and not over a large area, and it should not be used in the breast area during breastfeeding. How do you use Reparil N Gel?AdultsUnless otherwise directed, once or several times a day apply and spread over the skin over the diseased area. It is not necessary to massage in the gel, but it is possible if desired. Wash hands after use. Tell your doctor if the symptoms worsen or if the symptoms have not improved after 2 weeks. Children and adolescentsThe use and safety of Reparil N Gel in children and adolescents has not yet been tested. Stick to the dosage given in the package leaflet or as prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, Ref: or druggist. What side effects can Reparil N Gel have?The following side effects can occur when using Reparil N Gel: Frequency not known (cannot be estimated from the available data)allergic skin reactions (e.g. dry skin, skin redness, dermatitis, itching, hives, exfoliation of the skin) ; Hypersensitivity reactions (e.g. non-specific allergic reactions up to anaphylactic reactions; reactions of the respiratory tract, such as bronchospasm or shortness of breath; hypersensitivity reactions of the skin). If such symptoms occur, Care should be discontinued. If you get any side effects, talk to your doctor, Ref: or druggist. This also applies in particular to side effects that are not listed in this leaflet. What else needs to be considered?The Care product may only be used up to the date marked «EXP» on the container. Storage instructionsKeep out of the reach of children. Store at room temperature (15-25°C). Keep container tightly closed. Further informationYour doctor, Ref: or druggist can provide you with further information. These people have the detailed information for specialists. What does Reparil N Gel contain?100 g of gel contain:Active ingredientsAescin 1.0 g Diethylamine Salicylate 5.0 g Excipientspurified water, sodium edetate, carbomers, macrogol-6-glycerol-caprylocaprate, trometamol, 2-propanol, lavender oil, bitter orange blossom oil. Approval number51830 (Ref:) Where can you get Reparil N Gel? What packs are available?In pharmacies and drugstores, without a doctor's Ref:. Packs of 40g and 100g gel. Authorization holderMEDA Pharma GmbH, 8602 Wangen-Brüttisellen This leaflet was last checked by the Medicines Agency (Ref:) in July 2021. [REPA_nG_201D] ..
39.26 USD
Sidroga chamomile blossoms 20 bags 1.5 g
Sidroga Chamomile Blossoms 20 Bags 1.5 g..
11.63 USD
Traumeel ointment tube 50 g
TRAUMEEL ointment Tb 50 g - Product Description TRAUMEEL ointment Tb 50 g Looking for an effective ointment to alleviate pain and inflammation? TRAUMEEL ointment is here! Made with natural ingredients, this ointment is a reliable remedy for all kinds of pain, injuries, and swelling. It is a homeopathic medicine that is safe and gentle on the skin yet highly potent in providing quick relief. TRUAMEEL ointment is a must-have in everyone's medicine kit! Features: Contains natural ingredients, no synthetic compounds Used for treating a wide range of conditions Safe and suitable for adults and children Relieves pain, inflammation, and swelling effectively Non-greasy and easily absorbable Benefits: Quick and effective relief from pain and inflammation Promotes natural healing without harmful side-effects Soothes sore muscles and joints, reduces swelling and stiffness Can be used for sports injuries, sprains, bruises, strains, and many other conditions Provides a cooling sensation and an overall sense of relaxation Directions for Use: Apply a small amount of TRAUMEEL ointment to the affected area and gently massage until absorbed. Repeat 3 to 4 times daily or as directed by a healthcare professional. For external use only, avoid contact with eyes and open wounds. Precautions: Keep away from children Store in a cool and dry place Do not use if you are allergic to any of the ingredients Consult a healthcare professional if symptoms persist or worsen Ingredients: TRAUMEEL ointment contains a unique blend of natural compounds known for their Care, analgesic, and healing properties. The active ingredients include: Arnica montana, Calendula officinalis, Bellis perennis, and many others. For a full list, please refer to the package insert. Package: TRAUMEEL ointment is available in 50g tubes and comes in a convenient and hygienic packaging. ..
44.34 USD
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