Anatomical therapeutic chemical
(2 Pages)
Aqua dest braun rinse loes 6 ecotainer 1000 ml
Characteristics of Aqua Brown least rinse Lös 6 ecotainer 1000 mlAnatomical Therapeutic Chemical (АТС): V07ABCertified in Europe CEStorage temp min/max 15/25 degrees CelsiusAmount in pack : 6 mlWeight: 0.00000000g Length: 281mm Width: 195mm Height: 243mm Buy Aqua Brown least rinse Lös 6 ecotainer 1000 ml online from Switzerland..
59.10 USD
Artelac lipids edo gtt opht 30 monodos 0.6 g
Characteristics of Artelac lipid EDO Gd Opht 30 Monodos 0.6 gAnatomical Therapeutic Chemical (АТС): S01XA99Active ingredient: S01XA99Certified in Europe CEStorage temp min/max 15/25 degrees CelsiusKeep out of the sunAmount in pack : 30 gWeight: 72g Length: 29mm Width: 140mm Height: 75mm Buy Artelac lipid EDO Gd Opht 30 Monodos 0.6 g online from Switzerland..
47.13 USD
Axeta acetic alumina gel tb 50 g
Medical product with acetic acid clay What is Axeta and when is it used? The use of Axeta is recommended instead of moist compresses for all forms of minor, blunt (bloodless) injuries such as bruises, contusions, sprains and strains (without severe bruising) as well as skin abrasions and skin irritations, sunburn, insect bites and skin irritations caused by sweating ( burning feet) or sores.Axeta is available in a pleasantly cooling gel form and contains the well-known acetic clay (also known as acetic clay), supplemented by the caring properties of chamomile and arnica. Acetic tartaric clay protects the skin from the penetration of pathogens. Due to its cooling properties, Axeta helps relieve pain from blunt injuries and relieves itching from insect bites. The chamomile extract is used to care for sensitive and inflamed skin and the arnica tincture supports the natural regeneration of the skin. When should Axeta not be used or only with caution? Axeta should not be applied to open injuries (bleeding wounds). Axeta should not come into contact with the eyes or mucous membranes. Patients who know that they are hypersensitive to chamomile or arnica should not use the preparation. Inform your pharmacist or druggist if you suffer from other illnesses, have allergies, or are taking or using medicines (even those you bought yourself!) or use them externally. May Axeta be used during pregnancy or in the breastfeeding? Axeta can be used during pregnancy and breastfeeding. How do you use Axeta?Adults Axeta is extremely convenient to use. It has the pleasantly cooling and pain-relieving properties of wet poultices without the disadvantage of their cumbersome application.For minor inflammation and blunt injuries (swelling, sprains, etc.), apply gel thick, cover with gauze and fasten with a bandage. In the case of extensive skin inflammation, abrasions and sunburn, apply the gel in a thin layer and allow to dry or, on clothed parts of the body, cover with gauze before it dries completely.Observe the application described in the package leaflet or the application recommended by the pharmacist or druggist. Children and young people The use and safety of Axeta has not yet been tested in children and adolescents. What side effects can Axeta have? No side effects have been observed so far. If you do notice any side effects, you should inform your pharmacist or druggist. What else needs to be considered? Axeta may only be used up to the expiry date stated on the container.Keep out of the reach of children and at 15-25 °C. Axeta must not be taken. Keep the tube opening clean, close the tube after use. Your pharmacist or druggist can provide you with further information. What does Axeta contain? 1 g of Axeta fat-free gel contains 50 mg Aluminii acetatis tartratis solutio, 10 mg Chamomilla recutita extract, 10 mg Arnica montana tinctura. No artificial colors. Where can you get Axeta? Which packs are available? Available in pharmacies and drugstores. Tubes of 50 g and 100 g. Manufacturer Axapharm AG, Zugerstrasse 32, CH-6340 Baar. Status of the information February 2017...
27.75 USD
Becozym forte drag 20 pcs
What is Becozym forte and when is it used? Becozym forte contains seven important vitamins from the B group. Like all vitamins, the B group vitamins cannot be produced by the body itself, but must be ingested with food.The B group vitamins are part of very specific enzymes (ferments). They have the task of making carbohydrates, fats and protein from food usable for energy production, for the structure and function of nerves, blood, skin and mucous membranes as well as muscles. The interaction of the B group vitamins is of the utmost importance.Becozym forte contains the B group vitamins that the body needs. It is therefore used to prevent and treat existing vitamin B deficiencies, which can have the following causes:One-sided diet with light diets, slimming diets; Excessive alcohol consumption and a lack of appetite, such as occurs with feverish illnesses.Medicines that neutralize the vitamin effect. These include, in particular, preparations to fight severe infections (anti-infectives), preparations that inhibit the growth of cancer cells (cytostatics), and those that are taken to prevent epileptic seizures (anticonvulsants).Liver diseases that impair the incorporation of vitamins into the enzymes.Chronic alcoholism and its consequences, such as damage to the liver, heart and nervous system.What should be considered? For diabetics: 1 dragée contains 270 mg of carbohydrates = 4.6 kJ (1.1 kcal). Becozym forte contains lactose. When should Becozym forte not be taken? If you are allergic to one of the active ingredients or one of the excipients according to the composition, you must not take the preparation. When is Beco zym forte Caution required?Acute and chronic overdoses increase the risk of side effects. The intake of vitamins and minerals from other sources (fortified foods, diet supplements, or concomitant use of other medications) must be taken into account.Patients taking other vitamin products or medications, on a specific diet or under medical supervision must discuss the use of Becozym forte with their doctor, pharmacist or druggist.Patients with severe renal insufficiency must use Becozym forte discuss this with your doctor.If you need laboratory tests and are taking biotin, please tell your doctor. Biotin can affect the results.Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!)!Can Becozym forte be taken/used during pregnancy or breastfeeding?You can take vitamins and minerals during pregnancy in an amount that corresponds to your daily needs and take while breastfeeding. However, with daily doses such as those supplied with Becozym forte, you should only take this medicine after consulting your doctor.How do you use Becozym forte?The amount to be taken daily (daily dose) of the treatment depends on your age and the extent of the imminent or existing deficiency of vitamins from the B group. Unless otherwise specified by the doctor, pharmacist or druggist, the following guidelines apply to the dosage:Daily dose for prevention: Adults and adolescents from 12 years of age: 1 tablet once. Daily dose for treatment: Adults and adolescents from 12 years of age: 1 tablet two or three times. You can swallow the tablets whole with liquid. Becozym forte is not intended for use in children under 12 years of age doctor prescribed dosage. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Becozym forte have?The following side effects can occur after taking Becozym forte:Headache, allergic to anaphylactic reactions (skin reddening, skin rash, itching, swelling of the tissue (edema) or the face (angioedema), shortness of breath, asthma, diarrhea, drop in blood pressure, heart problems, anaphylactic shock).The urine may turn yellow while you are taking Becozym forte. The coloring is due to the excreted vitamin B2 (riboflavin) and is harmless.If you notice any side effects, contact your doctor, pharmacist 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 the medicine at room temperature (15-25 °C) and keep it out of the reach of children.Your doctor, pharmacist or druggist can provide you with further information tin, pharmacist or druggist. These people have the detailed technical information. What does Becozym forte contain? Active ingredients 1 dragee contains 15 mg vitamin B1 (thiamine nitrate), 15 mg vitamin B2 (riboflavin), 10 mg vitamin B6 (pyridoxine hydrochloride), 10 µg vitamin B12 (cyanocobalamin), 0.15 mg biotin, 25 mg calcium as active ingredients pantothenate, 50 mg nicotinamide. Excipients Arom.: Vanillinum, Ethylvanillinum et alia, Color: E 150c. Approval number 20407 (Swissmedic). Where can you get Becozym forte? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Dragées: 20 and 50. Authorization holder Bayer (Switzerland) AG, Zurich. This leaflet was last checked by the drug authority (Swissmedic) in December 2019....
11.12 USD
Daktarin cream 20mg/g tb 30g
What is Daktarin and when is it used? Daktarin Cream is used to treat skin infections caused by fungi, including yeasts and certain bacteria. Daktarin Cream is a washable emulsion. It is suitable for the treatment of fungal infections of the head, beard, body, feet, hands and groin area. Daktarin tincture is used to treat mild fungal infections on the front and side edges of the nail. If the nail bed is infected or if more than two nails are affected, you should consult your doctor before use. What should be considered? Wash your hands carefully after each use, unless the treatment is for the hands. Use your own washcloth and towels to prevent transmission to others. Change the clothing that comes into contact with the affected area of skin regularly, e.g. change stockings (no synthetic fibres) frequently if you have athlete's foot. Avoid reinfection or transmission in residential areas and public places (e.g. swimming pools).When should Daktarin not be used?Do not use Daktarin cream or tincture if you have a known sensitivity to these medicines or to other similar antifungals.When should you be careful when using Daktarin?Daktarin can cause severe allergic reactions cause reactions. Watch out for signs of an allergy during treatment with Daktarin (see the section «What side effects can Daktarin have?»).In the event of extensive fungal infestation or if the nails are also infested, the doctor must be consulted.Daktarin cream and tincture must not come into contact with the eyes or mucous membranes.Daktarin tincture should not be applied to open wounds or mucous membranes due to the alcohol content. If you are taking a blood thinner or other medicines, consult your doctor or pharmacist before using Daktarin. The effects and side effects of some other medicines may be increased if taken at the same time as miconazole.Inform your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies ortake or use external medicines (including those you have bought!)!May Daktarin can be used during pregnancy or breastfeeding? Daktarin cream and tincture must not be used during pregnancy and breastfeeding unless prescribed by a doctor. How do you use Daktarin? Before using Daktarin, the affected skin areas should be cleaned and dried carefully. For successful treatment, you must use Daktarin daily. The treatment must be carried out continuously until the skin changes are no longer visible. If the symptoms worsen or if there is no improvement within approx. 2 weeks or after 4 weeks in the case of athlete's foot, you should consult your doctor. Another skin disease could be the cause.Daktarin CreamAdults and children from 2 yearsApply Daktarin Cream twice a day to the affected area and rub in lightly with your fingers. Duration of use: 2-6 weeks. The treatment should be continued for at least 1 week after the symptoms have disappeared. Children under 2 years of age In children under 2 years of age, Daktarin Crème should only be usedauml;ss medical prescription. Daktarin tincture Adults and adolescents from the age of 12 Only use Daktarin tincture after medical clarification. The nail should be cut as short as possible. For nail fungus, apply a layer of Daktarin tincture to the affected nail and the surrounding tissue twice a day and allow to dry (a film forms). It is recommended to clean the nail and surrounding tissues with acetone before each new application. Treatment must be continuous until the nail has fully regenerated, which generally takes several (2-3) months.Children under 12 years of ageThe use and safety of Daktarin tincture in children under 12 years of age has not been established.Respect the dosage provided 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, pharmacist or druggist.What side effects can Daktarin have?Severe allergic reactions have been observed in connection with Daktarin. Signs of a severe allergic reaction may include:swelling of the face, lips, mouth, tongue or throat and/ordifficulty swallowing or breathing and/or severe skin rash, itching, hivesIf any of these allergic reactions occur, stop using Daktarin and contact your doctor or pharmacist immediately.The following side effects may occur when using Daktarin cream and tincture:Light patches of skin (pigmentation disorder), reddening of the skin, skin irritation, skin burning, skin inflammation, warming of the skin or itching may occasionally occur at the application site.Hives, contact dermatitis or other skin rashes occur very rarely.If you notice side effects, contact your doctor, pharmacist or druggist or Your doctor, pharmacist 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.Store Daktarin cream and tincture at room temperature (15–25 °C). Keep out of the reach of children!Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Daktarin contain?Active substances Cream: miconazole nitrate 20 mg/g. Tincture: miconazole 20 mg/ml. Excipients Cream: antioxidant: butylhydroxyanisole (E 320) and preservative: benzoin acid (E 210). Tincture: alcohol, propylene glycol. Authorization number 37063, 43893 (Swissmedic). Where can you get Daktarin? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Daktarin Cream: Pack of 30 g. Daktarin Tincture: Pack of 30 ml. Authorization holder Janssen-Cilag AG, Zug, ZG authority (Swissmedic)...
37.20 USD
Delima feminin vag supp 15 pcs
The Delima Feminin vaginal suppositories contain a combination of vegetable oils. The oils, especially the pomegranate seed oil, lead to a soothing gliding effect and moisture in the vaginal area. Many women suffer from vaginal dryness, especially during the menopause. With the Delima Feminin vaginal suppositories, women can enjoy a pleasurable and carefree intimate life even during menopause. As a lubricant, the direct use of vaginal suppositories is always recommended when needed. Just a few minutes after insertion, the suppository has melted pleasantly and imperceptibly. Application Insert the vaginal suppository into the vagina and wait about 5 minutes for the suppository to dissolve. The lubricity of the oils covers the lack of moisture in the vagina for about half an hour. Remove any escaping oil with a cosmetic tissue. Composition Hard fat, grape seed oil, pomegranate seed oil, natural vitamin E (tocopherol)...
47.47 USD
Fenivir cream tb 2g
What are Fenivir cream and tinted cream and when are they used? Fenivir cream and tinted cream are used for the local treatment of cold sores on the lips (= herpes labialis). They belong to the group of drugs that are effective against viruses.What should be considered?The active ingredient in Fenivir cream and tinted cream is not effective against all microorganisms that cause infectious diseases. Using an incorrectly chosen or incorrectly dosed drug can cause complications. Therefore, never use the preparation yourself to treat other diseases or other people.When should Fenivir cream or tinted cream not be used?Fenivir cream or tinted cream should not be used if there is a known hypersensitivity to the active ingredients penciclovir, famciclovir or one of the excipients, e.g. propylene glycol.When should caution be exercised when using Fenivir cream or tinted cream? Fenivir cream or tinted cream should not be used on mucous membranes (e.g. in the mouth or genital area) or in the eye.Patients with a weakened immune system should only use Fenivir cream or tinted cream as prescribed by a doctor.If you are not sure what is causing the blister, infection or injured area, then consult your doctor .Fenivir cream and tinted cream have not been tested for use in children under 12 years of age and should therefore not be used in children under 12 years of age.Inform your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies orother medicines (also self-bought!) or use externally!Can Fenivir cream or tinted cream be used during pregnancy or while breastfeeding?During pregnancy and breastfeeding, Fenivir cream or tinted cream must not be used unless prescribed by a doctor. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding, or ask your doctor, pharmacist or druggist for advice.How do you use Fenivir cream or tinted cream?It is important to start treatment with Fenivir cream or tinted cream as soon as possible after the first symptoms appear (e.g. burning, itching).Adults, Elderly patients and adolescents from the age of 12: Apply Fenivir cream or tinted cream to the affected areas of the lips and face with a clean finger during the day (after getting up until going to bed) about every 2 hours. Fenivir Cream or Tinted Cream can be applied with a cotton swab. Wash your hands before and after applying the cream. The treatment period is 4 days. If the disease worsens or the cold sore does not heal after 4 days, the doctor should be consulted. Children: Fenivir Cream or Tinted Cream should not be used in children under the age of 12, as the preparations have not been tested for use in children under the age of 12. Hint How to use and duration of treatment: It has been shown that starting treatment with Fenivir cream or tinted cream even after the blisters have formed accelerates their healing, reduces pain and shortens viral shedding. Adhere to the treatment period of 4 days even if you have already improved beforehandfeel it and do not stop treatment if you do not see an improvement immediately. Insufficient duration of use or stopping treatment too early can result in the disease flaring up again. If you forget to apply the cream at the scheduled time, do so as soon as possible. The following applications should be done every 2 hours. If you apply a large amount of the cream to the skin at once, no harmful effects are to be expected apart from slight skin irritation. If you have accidentally swallowed Fenivir cream or tinted cream, no harmful effects are to be expected apart from irritation of the oral mucosa. In both cases, no special treatments are necessary. If you still have concerns, please contact your doctor, pharmacist or druggist. Observe the dosage specified in the package leaflet or as prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Fenivir cream or tinted cream have?The following side effects may occur when using Fenivir cream or tinted cream: Fenivir cream or tinted cream may cause reactions at the administration site in some patients, e.g. temporary burning sensation en, stinging or numbness. Rarely, hypersensitivity reactions such as hives, facial swelling and skin rashes can occur: In these cases, the treatment should be discontinued and the doctor consulted immediately.If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist.What else should be observed?Keep out of the reach of children in the original packaging . Do not store above 30°C. The medicinal product may only be used up to the date marked «EXP» on the container.Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for professionals. What does Fenivir cream or tinted cream contain? 1 gram of Fenivir cream contains 10 mg penciclovir, the excipient propylene glycol and other excipients. 1 gram of Fenivir tinted cream contains 10 mg penciclovir, the excipient propylene glycol and other excipients and the dye iron oxide red and yellow (E172).Approval number 53680, 62647 (Swissmedic). Where can you get Fenivir Cream and Tinted Cream? What packs are available? Fenivir cream 2 g tube: In pharmacies and drugstores, without a doctor's prescription.Fenivir tinted cream 2 g tube: In pharmacies and drugstores, without a doctor's prescription.Marketing authorization holderInterdelta SA, 1762 Givisiez. This leaflet was last checked by the drug authority (Swissmedic) in January 2017...
26.69 USD
Gelodurat caps 30 pcs
What is GeloDurat and when is it used? GeloDurat contains 300 mg distillate of essential oils from various plants and is used for acute and chronic bronchitis as well as inflammation of the paranasal sinuses (acute and chronic sinusitis). GeloDurat liquefies the mucus in the bronchi and paranasal sinuses, promotes the evacuation of this mucus and makes it easier to expectorate. Ge loDurat reduces the aggravation of the disease that is common in chronic courses.What should be considered?Support the expectorant effect of GeloDurat by drinking a lot.When should GeloDurat not be taken or should only be taken with caution?GeloDurat should not be taken if you are hypersensitive to one of the ingredients of the drug.Do not use in small children under 4 years of age. Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (including 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 scientific state of the art that Gelo Durat can also be taken during pregnancy without any 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?In the case of 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 treatment. GeloDurat capsules should be swallowed whole half an hour before eating with plenty of cold liquid. Only use in children under the age of 10 if prescribed by a doctor. Do not use in small children under 4 years of age. To make coughing up in the morning easier in the case of chronic bronchitis, you can also take one GeloDurat capsule in the evening before going to bed. To make it easier to get a good night's sleep, the last dose can be taken before going to bed. In the case of respiratory diseases that last longer than 7 days, a doctor, pharmacist or druggist must be consulted. Follow the dosage given in the package leaflet or prescribed by your doctor. If you believe that the medicine works too weak or too strong, speak to your doctor, pharmacist or drugstore, pharmacist. What side effects can have gelodurate? Z, cause diarrhea and flatulence. If kidney stones or gallstones are present, they can be set in motion. In individual cases, hypersensitivity reactions (e.g. skin rash, facial swelling, shortness of breath or circulatory disorders) have been reported. If you notice side effects that are not described here, you should inform your doctor, pharmacist or pharmacist. What else needs to be considered? Gelo Do not store Durat above 25 °C. Store in the original packaging and the outer carton. The medicine may only be used up to the mbe used on the date marked «EXP».Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does GeloDurat contain?1 gastro-resistant capsule contains 300 mg distillate from essential oils of eucalyptus and myrtle leaves as well as sweet orange and lemon peel.This preparation also contains auxiliary substances.Authorization number55928 (Swissmedic).Where can you get GeloDurat? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Packs with 30, 60 and 120 capsules. Authorization holder Gebro Pharma AG, CH-4410 Liestal. Manufacturer G. Pohl-Boskamp GmbH & Co. KG, D-25551 Hohenlockstedt.This leaflet was last checked by the drug authority (Swissmedic) in September 2005...
26.96 USD
Hirudoid forte gel 4.45mg/g tb 100g
AMZV What is Hirudoid forte Gel and when is it used? Hirudoid forte Gel contains the active ingredient mucopolysaccharide polysulphate (heparinoidum MPS). This prevents the formation of blood clots and promotes their regression. In addition, inflammatory processes and fluid accumulations in the tissue are eliminated.After using Hirudoid forte Gel, tissue tension and the associated pain decrease, swelling and bruising decrease, the heaviness in the legs is relieved.Hirudoid forte Gel is used:for complaints related to varicose veins such as pain, feelings of heaviness, swollen legs (stasis oedema);for muscle pain and se for blunt sports injuries and accidental injuries such as contusions, contusions, strains, with hematoma (bruise) and swelling.The gel has a cooling effect.On medical prescription, Hirudoid forte Gel can alsofor (superficial) phlebitis;for inflammatory conditions in varicose veins;for the aftercare of sclerotherapy as well as for the supportive treatment of venous thrombosis.What should be considered?You can support the treatment of your venous disease by ensuring sufficient exercise. Sitting or standing for long periods of time causes congestion and strains your veins. Also avoid additional stress such as alcohol and cigarettes in excess, heavy or flatulent food, obesity and overheating from sunbathing and excessive use of the sauna. Also follow the advice of your doctor that goes beyond the use of Hirudoid, such as e.g. gymnastics or wearing support stockings. When should Hirudoid forte Gel not be used? Hirudoid forte Gel should not be used in patients with a known hypersensitivity to heparinoid or any of the other excipients.When is caution required when using Hirudoid forte Gel?Hirudoid forte Gel may only be used on intact skin. Please make sure that the gel does not come into contact with open wounds, eyes or mucous membranes. In the case of venous diseases that are due to the presence of a blood clot (so-called thromboembolism), must be massaged. If your symptoms persist for a longer period of time or if the symptoms worsen, you should definitely consult a doctor. Inform your doctor, pharmacy r or druggists or your doctor or pharmacist if you suffer from other diseases, have allergies or take other medicines (including those you bought yourself!) or use them externally!Can Hirudoid forte Gel be used during pregnancy or while breastfeeding?Based on previous experience, there is no known risk to the unborn child if used as intended. However, systematic scientific investigations have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding or ask your doctor, pharmacist or druggist for advice.How do you use Hirudoid forte Gel?AdultsUnless otherwise prescribed by the doctor, apply a strand of gel of 3-5 cm several times a day (or more if necessary). In the case of thromboembolic diseases (blood clots), however, must be massaged. With the 100 g tube, only about a third of the specified length of the gel strand (i.e. 1-2 cm) should be used for the 100 g tube due to the larger tube opening. As with all gels containing alcohol, you should not put a bandage on Hirudoid forte Gel. Hirudoid forte cream is available for use under bandages.ChildrenThe use and safety of Hirudoid forte gel in children has not been systematically tested to date.Observe the instructions given in the leaflet ordosage prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Hirudoid forte Gel have?The following side effects can occur when using Hirudoid forte Gel:In rare cases, hypersensitivity reactions of the skin (allergy) can occur.Inform them Tell your doctor if you notice any signs. You should no longer use Hirudoid forte Gel if you experience severe irritation. If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered? The aluminum foil at the opening of the tube can be easily pierced with the spike in the cap. Hirudoid forte Gel may only be used up to the must be used by the date marked «EXP» on the tube. Medicines should be stored in a dry place and out of the reach of children. Store at room temperature (15–25 °C). Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Hirudoid forte Gel contain?1 g of gel contains:Active substance: Mucopolysaccharide polysulfate (Heparinoidum MPS) 4.45 mg (equivalent to 400 U.).Excipients: Propylene glycol and other excipients.Approval number40550 (Swissmedic).Where can you get Hirudoid forte Gel? What packs are available? Hirudoid forte Gel is available in pharmacies and drugstores without a doctor's prescription. There are packs of 40 g and 100 g Gel. Authorization holder Medinova AG, 8050 Zurich. This package leaflet was last published in February 2008 by the drug authority (Swissmedic ) checked...
64.41 USD
Hirudoid gel 3mg/g tb 40g
Characteristics of Hirudoid Gel 3 mg / g Tb 40 gAnatomical Therapeutic Chemical (АТС): C05BA01Storage temp min/max 15/25 degrees CelsiusAmount in pack : 1 gWeight: 0.00000000g Length: 0mm Width: 0mm Height: 0mm Buy Hirudoid Gel 3 mg / g Tb 40 g online from Switzerland..
15.08 USD
Lacdigest chewable tablets 100 pcs
AMZV What is Lacdigest and when is it used? Lacdigest is an enzyme preparation. It contains the enzyme tilactase, which is necessary for the breakdown of lactose (milk sugar). Eating lactose-containing foods such as milk, cheese, butter and yoghurt, as well as sauces, bouillon, ice cream and lactose-containing tablets can lead to flatulence, abdominal pain and diarrhea. The reason lies in a reduced activity of the body's own enzyme, which normally breaks down lactose in the intestine so that the breakdown products can be absorbed by the body. Lacdigest enables the breakdown of lactose in the gastrointestinal tract. This means that lactose-containing foods can also be digested by patients with lactose intolerance.What should be considered?Lacdigest is not effective if you are allergic to milk proteins.When should Lacdigest not be used?Lacdigest should not be used if there is a known allergy to tilactase, which is obtained from Aspergillus oryzae. Age limit for children see «How do you use Lacdigest?».When should you be careful when taking Lacdigest?If used as directed, no special precautions need to be followed. Tell your doctor or pharmacist if you suffer from other illnesses, have allergies or if you take other medicines (including those you bought yourself!) or use them externally!Can Lacdigest be used during pregnancy or while breastfeeding?Lacdigest is only effective in the gastrointestinal tract. The enzyme is not absorbed into the blood. Based on previous experience, there is no known risk for the child when used as intended.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 or pharmacist for advice.How do you use Lacdigest?The dosage depends on the severity of the symptoms that occur with lactose intolerance and on the amount of lactose ingested. Unless otherwise prescribed by the doctor, the following guidelines apply:Children from 3 years and adults: 1 chewable tablet per 5 g of lactose, corresponding to 1 chewable tablet per 1 dl of milk. If the symptoms are not reduced, the dose can be increased.Maximum single dose: 6 chewable tablets per mealMaximum daily dose: 12 chewable tablets per dayThere is no experience with the use of Lacdigest in children under the age of 3 years. The chewable tablets must be chewed immediately before taking a lactose-containing meal.They can also be swallowed. 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 or pharmacist.What side effects can Lacdigest have?The following side effects can occur when taking Lacdigest: Allergic reactions in the event of hypersensitivity to the enzyme tilactase, which is obtained from the Aspergillus oryzae fungus.In this case, Lacdigest should no longer be taken become. If you notice any side effects that are not described here, you should inform your doctor or pharmacist. What else needs to be considered? Lacdigest should be stored in a dry place at room temperature (15-25°C) and out of the reach of children. The medicinal product may only be used up to the date marked “EXP” on the container. If you have chewable tablets that have expired, please return them to your pharmacy for disposal. Your doctor or pharmacist can provide you with further information. These people have the detailed technical information.What does Lacdigest contain?Active ingredient: Lacdigest containsml;lt 60 mg tilactase from Aspergillus oryzae in one chewable tablet.Excipients: Pregelatinized starch, microcrystalline cellulose, glucose monohydrate, anhydrous glucose, calcium carmellose stearate, magnesium stearate, sodium citrate,Authorization number53055 (Swissmedic)Where can you get Lacdigest? What packs are available?In pharmacies without a doctor's prescription. There is a pack of 50 and 100 chewable tablets.Authorization holderRecordati AG, 6340 BaarThis leaflet was last checked by the drug authority (Swissmedic) in June 2009...
71.47 USD
Maltofer fol chewing tablets 30 pcs
What are Maltofer Fol chewable tablets and when are they used? Maltofer Fol chewable tablets are a combination preparation containing iron and folic acid. They are used to treat and prevent iron deficiency with an increased need for folic acid during pregnancy and breastfeeding.Iron is an essential component of the red blood pigment, the red muscle pigment and the iron-containing enzymes. Folic acid is an important vitamin for the development of the unborn child. A lack of folic acid in the first few weeks of pregnancy can lead to birth defects in the child. What should you watch out for? Before you start taking Maltofer Fol chewable tablets, the blood's iron and blood pigment (haemoglobin) content should have been clarified by the doctor through suitable tests. If the symptoms are not caused by iron deficiency, Maltofer Fol Chewable Tablets are not effective.Your doctor will want to check the progress of your treatment through regular examinations and may also carry out blood tests. This is normal and should not concern you. If your symptoms do not improve within 3 weeks, consult your doctor.During treatment with Maltofer, the stool may become darkened, but this is harmless.When should Maltofer Fol chewable tablets not be taken/used?If you have a known hypersensitivity (allergy) or intolerance to the active ingredients iron(III) hydroxide polymaltose Complex and folic acid or one of the excipients (see "What does Maltofer Fol chewable tablets contain?")In the case of excess iron in the body (e.g. due to rare iron storage diseases which lead to iron deposits in the tissues)In the case of so-called iron utilization disorders (if the anemia is due, for example, to insufficient utilization of iron)In the case of anemia that is not due to an iron deficiency (e.g. due to increased depletion of hemoglobin or lack of vitamin B12).When is caution required when taking / using Maltofer Fol chewable tablets?Before taking Maltofer Fol, tell your doctor, pharmacist or druggist if you have the following:An infection or a tumor.A vitamin B deficiency 12. The folic acid contained in Maltofer Fol can mask a lack of vitamin B12.Tell your doctor, pharmacist or druggist if you are being treated with any of the following medicines:Injectable iron preparations. Such iron preparations should not be used at the same time as Maltofer Fol.Drugs used to treat epilepsy, especially phenytoin.Chloramphenicol, a drug used to treat bacterial infections. Your doctor will monitor you carefully if you are taking both medicines.Tell your doctor, pharmacist or druggist if you have received blood transfusions as there is a risk of iron overload with supplemental iron.This medicine contains 10 mg sodium (main component of cooking/table salt) per tablet. This is equivalent to 0.5% of the recommended maximum daily dietary intake of sodium for an adult.No studies have been conducted. However, it is unlikely that Maltofer Fol will have any effect on the ability to drive and use machines.Tell your doctor ifPharmacist or druggist or your doctor if you:Suffer from other diseasesHave allergiesTake other medicines (including those you bought yourself!).Can Maltofer Fol chewable tablets be taken/used during pregnancy or while breastfeeding?If you are pregnant, want to become pregnant or are breastfeeding en, you may only take Maltofer Fol after consulting your doctor.How do you use Maltofer Fol chewable tablets?Maltofer Fol chewable tablets can be chewed or swallowed whole and should be taken during or immediately after meals. Maltofer Fol chewable tablets have a break line on one side. This is only to break the pills for easier swallowing, not to split the pills into two equal doses. The daily dose can be divided into single doses or taken all at once. For the prevention and treatment of iron deficiency without anemia and to cover an increased need for folic acid: 1 chewable tablet daily. For the treatment of iron deficiency with anemia and to cover an increased need for folic acid: 2-3 tablets daily. When the blood test values for hemoglobin are normal again, the treatment is started with 1 Chewable tablets continued daily until the end of pregnancy to cover the increased need for iron and to replenish iron stores. Maltofer Fol chewable tablets are not suitable for children aged 12 years and younger. The dosage and duration of treatment depend on the extent of the iron deficiency. The doctor decides on the exact duration of treatment in each case. If you have taken more Maltofer Fol than you should, talk to your doctor, pharmacist or druggist. Too high a dose of folic acid could cause mood disorders, changes in sleep patterns, irritability and hyperactivity, nausea, abdominal distension and flatulence.If you forget to take Maltofer Fol, simply take the next dose at the usual time. Do not take a double dose to make up for a missed dose.Stick to the dose 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, pharmacist or druggist.What side effects can Maltofer Fol chewable tablets have?The following side effects can occur when taking Maltofer Fol chewable tablets:Very common (affects more than 1 in 10 users): a very common side effect is discoloration of the stool caused by iron excretion, but this is harmless. Common (affects 1 to 10 users in 100): commonly observed side effects are nausea, constipation, diarrhea and abdominal pain. Uncommon (affects 1 to 10 users in 1000): occasionally vomiting, discoloration of the teeth, inflammation of the stomach (gastritis), itching, rash, hives, reddening of the skin (erythema ) and headaches. Rare (affects 1 to 10 users in 10,000): in rare cases, patients suffer from muscle cramps and muscle pain (myalgia). These side effects are usually temporary. If you notice side effects, contact your doctor, pharmacist 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 medicinal product may only be used up to the point on the containerdate marked «EXP».Storage instructionsStore at room temperature (15-25°C).Keep out of the reach of children.Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for professionals.What does Maltofer Fol chewable tablets contain?Active ingredients1 Maltofer Fol chewable tablet contains 100 mg iron in the form of iron(III) hydroxide polymaltose complex and 0.35 mg folic acid.ExcipientsTallow, macrogol 6000, anhydrous starch hydrolyzate, microcrystalline cellulose, Chocolate flavor, sodium cyclamate, vanillin, cocoa powder.Authorization number46538 (Swissmedic)Where can you get Maltofer Fol chewable tablets? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Maltofer Fol chewable tablets are available in packs of 30 or 100 chewable tablets. Authorization holder Vifor (International) AG 9001 St. Gallen This package leaflet was last published in September 2021 by the drug authority (Swiss medic)...
20.48 USD
Medihoney medical honey antibacterial 50g
Characteristics of Medihoney Medical Honey Antibacterial 50gAnatomical Therapeutic Chemical (АТС): D03AX99Active ingredient: D03AX99Certified in Europe CEStorage temp min/max 15/25 degrees CelsiusAmount in pack : 1 gWeight: 77g Length: 38mm Width: 50mm Height: 125mm Buy Medihoney Medical Honey Antibacterial 50g online from Switzerland..
103.71 USD
Microlax klist 4 tb 5ml
What is Microlax and when is it used? Microlax is a product for rectal use. The active components of Microlax together lead to a softening of the stool and the bowels are gently emptied within 5 - 20 minutes.Microlax is used for short-term use in cases of hardened stool and the resulting constipation of the lower sections of the intestine, to facilitate stool movement in case of stool thickening, before and after operations and as a stool aid during pregnancy, before birth, in childbirth and while breastfeeding.When should Microlax not be used ? Microlax must not be used in case of hypersensitivity to one of the ingredients. When is caution required when using Microlax? Long-term or high-dose use can result in loss of water and minerals (potassium) and damage to the intestinal mucosa with increased intestinal sluggishness. Contains sorbic acid (E 200): Can cause localized skin irritation (e.g. contact dermatitis). .Inform your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally!See a doctor if symptoms persist or become worse and do not use Microlax for a long time clean up.Can Microlax be used during pregnancy or while breastfeeding?Based on previous experience, there is no known risk for the child if used as directed. However, systematic scientific investigations have never been carried out. As a precaution, you should avoid taking medicines during pregnancy and breastfeeding, or ask your doctor, pharmacist or druggist for advice.How do you use Microlax?Break off the tip.Adults and children over 3 years of age: In adults and children over 3 years of age, the cannula is fully inserted.Children under 3 years of age: In children under 3 years of age, the cannula is only inserted up to half of its length. Please pay attention to the marking ring on the cannula. A drop of the contents of the tube, applied to the cannula, is sufficient as a lubricant. In stubborn cases, 2 tubes may be needed. The effect usually occurs after 5-20 minutes.Stick to 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, pharmacist or druggist.What side effects can Microlax have?The following side effects have been reported with the use of Microlax, although the frequency of the side effects is unknown: Hypersensitivity reactions (e.g. itching, reddening of the skin, swelling in the ear, hives), pain and discomfort in the Abdomen, discomfort in the area of the anus, loose stools.If you notice side effects, contact your doctor, pharmacist 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 drug may only be used up to the date marked "EXP" on the package.Storage instructionsStore at room temperature (15 - 25°C). Keep out of the reach of children.Your doctor, pharmacist or druggist can provide you with further information, Apotheker or druggist. These people have the detailed technical information. What does Microlax contain? Active substances Sodium citrate dihydrate 90 mg, sodium dodecylsulfoacetate 9 mg, sorbitol 625 mg per 1 ml solution. Excipients Sorbic acid (E 200), glycerol, purified water. Approval number29869 (Swissmedic).Where can you get Microlax? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Disposable enema with 5 ml solution: packs of 4, 12 and 50 tubes. Authorization holder Janssen-Cilag AG, Zug, ZG This package leaflet was last checked by the drug authority (Swissmedic) in August 2021 ...
15.83 USD
Modules ibd plv ds 400 g
Characteristics of Modules IBD PLV Ds 400 gAnatomical Therapeutic Chemical (АТС): V06DBActive ingredient: V06DBStorage temp min/max 15/25 degrees CelsiusAmount in pack : 1 gWeight: 524g Length: 104mm Width: 104mm Height: 144mm Buy Modules IBD PLV Ds 400 g online from Switzerland..
72.70 USD
Mucokehl gtt opht d 5 fl 5 ml
When is Mucokehl D5 eye drops used? According to the homeopathic drug picture, Mucokehl® D5 eye drops can be used on the eyes for circulatory disorders. What should you bear in mind? If your doctor has prescribed other medicines for you, ask your doctor or pharmacist whether Mucokehl® D5, Eye drops may be used at the same time. If there is no improvement after 2-3 days of treatment, professional advice should be sought. If you feel pain in your eyes, notice visual disturbances or reddening of the eyes, you should consult an ophthalmologist immediately. If an irregular pulse, severe palpitations, stabbing pains in the chest area and shortness of breath occur suddenly or last longer, you should consult a doctor. You will find out whether the heart or the vessels are organically diseased or whether the symptoms are caused by nerves.When should Mucokehl D5 eye drops not be used or should only be used with caution?Mucokehl® D5 eye drops should not be used in the case of hypersensitivity to penicillin and chlorhexidine acetate (preservatives). Mucokehl® D5, eye drops may only be used in children if expressly prescribed by a doctor. Tell your doctor or pharmacist if you- suffer from other diseases- have allergies or- take other medicines (including those you bought yourself) or use them on your eyes.May Mucokehl D5 eye drops be taken/used during pregnancy or breastfeeding?How do you use Mucokehl D5 eye drops?case Unless otherwise prescribed by the doctor, drip 1 drop into the eye to be treated twice a day. Do not touch the pipette tip. Close bottle immediately after use. After opening the pack, the eye drops may be used for a maximum of 1 month. Follow the dosage given in the package leaflet or prescribed by your doctor. If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with him or her. If you think the medicine is too weak or too strong, talk to your doctor or pharmacist.What side effects can Mucokehl D5, eye drops have?The following side effects can occur when using Mucokehl® D5, eye drops: In very rare cases, allergic reactions to one of the ingredients (active ingredient, preservative). The drug must be discontinued immediately and the doctor must be consulted immediately. If you notice any side effects that are not described here, tell your doctor or pharmacist. When using homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, discontinue Mucokehl® D5, eye drops and inform your doctor or pharmacist. What else should be observed? The drug may only be used up to the date marked "Use by" on the container. Store drug out of reach of children. Store at room temperature (15-25°C). Your doctor or pharmacist can provide you with further information. What does Mucokehl 5X eye drops contain? The eye drops contain: Mucor racemosus 5X aquos dilutio (HAB; 5a). This preparation also contains isotonic saline solution and the preservative chlorhexidine acetate as auxiliary substances. Approval number46731 (Swissmedic)Where to getn you Mucokehl D5, eye drops? What packs are available? In pharmacies without a doctor's prescription. 5 mL dropper bottle. Authorization holder ebi-pharm ag, Lindachstr. 8c, 3038 KirchlindachThis leaflet was last checked by the drug authority (Swissmedic) in February 2004...
26.62 USD
Nasal ointment rüedi spirig hc nasal ointment tb 20 g
What is Rüedi Spirig HC nasal ointment and when is it used? Rüedi Spirig HC nasal ointment is used to moisten dry nasal mucosa. It contains the two active ingredients menthol and camphor. By stimulating cold-sensitive nerve endings, these have a cooling, pain-relieving and itching-relieving effect. Nasal ointment Rüedi Spirig HC is therefore used:For damaged nasal mucosa, e.g. after long-term treatment with decongestants.For dry mucous membranes as a result of staying in air-conditioned rooms or in a dry environment.For dry nasal catarrh with mucosal inflammation.In the case of occupational irritation of the nasal mucosa.What should be considered?If you have problems with the nasal mucosa, you should make sure that the humidity in your living and working space is sufficient, especially in winter. Prolonged use of mucosal decongestants should be avoided.When should nasal ointment Rüedi Spirig HC not be used or only with caution?Nasal ointment Rüedi Spirig HC should not be used on infants. The preparation should be used with caution in small children. Inform your doctor, pharmacist or druggist or your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!) or use them externally.How do you use Rüedi Spirig HC nasal ointment?To be used in adults and children from the age of 6 years: apply some ointment in both nostrils several times a day en and then gently massage the nose externally. Observe the dosage given in the package leaflet or prescribed by the doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.What side effects can Rüedi Spirig HC nasal ointment have?The following side effects can occur when using Rüedi Spirig HC nasal ointment:Rüedi Spirig HC nasal ointment contains essential oil and camphor, which can lead to irritation of the mucous membranes and respiratory disorders in sensitive patients.Rüedi Spirig HC nasal ointment contains the auxiliary substance butylhydroxyanisole (E 320), which can cause localized skin irritation (e.g. contact dermatitis), irritation of the eyes and mucous membranes.Rüedi Spirig HC nasal ointment contains the auxiliary substance wool wax (lanolin), which can cause localized skin irritation (e.g . contact dermatitis). Rüedi Spirig HC nasal ointment contains the auxiliary agent cetostearyl alcohol, which can cause localized skin irritation (e.g. contact dermatitis).Rüedi Spirig HC nasal ointment contains the auxiliary substances methyl (4-hydroxybenzoate) (E 218) and propyl (4-hydroxybenzoate), which can cause allergic reactions, including delayed reactions.If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist.What else is there to be observed? Keep at room temperature (15-25 °C) and out of the reach of children. The medicinal product may only be used up to the end of the period marked “EXP.” on the container. designated date.Your doctor, pharmacist or druggist can provide you with further information.What does Rüedi Spirig HC nasal ointment contain?1 g nasal ointment containsActive ingredients:2 mg peppermint oil, 4 mg camphor oil 10%.Excipients:white vaseline, viscous paraffin, cetostearyl alcohol 16mg, wool wax (lanolin) 40mg, methyl (4-hydroxybenzoate) (E 218) 2mg, propyl (4-hydroxybenzoate) 2mg, butylated hydroxyanisole (E 320) 0.1mg, purified water.Approval number..
14.62 USD
Ostenil plus inj lös 40 mg/2ml fertspr
Characteristics of Ostenil Plus Inj Loes 40 mg / 2ml FertsprAnatomical Therapeutic Chemical (АТС): M09AX01Active ingredient: M09AX01Certified in Europe CEStorage temp min/max 15/25 degrees CelsiusAmount in pack : 1 piecesWeight: 0.00000000g Length: 0mm Width: 0mm Height: 0mm Buy Ostenil Plus Inj Loes 40 mg / 2ml Fertspr online from Switzerland..
164.72 USD
Reduforte biomed tabl 60 pcs
Medical device What is Reduforte Biomed and when is it used? Reduforte Biomed is used for weight control and for the prevention and treatment of obesity.Reduforte Biomed reduces calorie intake from the main nutrients carbohydrates, sugar and fat. It contains Clavitanol? IQP VV 102, a patented plant-derived complex that reduces the breakdown of these nutrients in the gastrointestinal tract, thereby reducing calorie intake. This is how Reduforte Biomed helps you lose 4 times more weight than diet and exercise alone. The effect is clinically proven. In addition, the reduced carbohydrate intake lowers the blood sugar level, which helps control blood sugar levels and reduces food cravings. What should you be aware of? It is recommended to take Reduforte Biomed 2 hours before or after other preparations or medicines.If you are in doubt as to whether you can take Reduforte Biomed and/or use it in combination with a medicine, or if you have general health problems, please consult your doctor, pharmacist or Druggists before taking Reduforte Biomed.While taking Reduforte Biomed is an important step in controlling your weight, it should always be considered as part of an overall weight management plan. When should Reduforte Biomed not be used or when should be used with caution? Children and adolescents between 12 and 18 years of age should only use the product on the advice of a healthcare professional.Do not use Reduforte Biomed not if your BMI (Body Mass Index) is below 18.5.Because Reduforte Biomed can affect blood sugar levels, diabetics may need to adjust their treatment to avoid hypoglycaemia. Please ask your doctor before taking Reduforte Biomed.Do not use Reduforte Biomed if you are hypersensitive to grapes or corn or products made from them, or if you are allergic to any of the ingredients listed. Can Reduforte Biomed be taken if you are pregnant or breastfeeding? Do not use Reduforte Biomed if you are pregnant or breastfeeding. How do you use Reduforte Biomed? Recommended for adults over 18 years of age. Take 2 tablets with sufficient liquid 30 minutes before the 2 heaviest meals of the day. Adequate liquid intake of at least 2 liters daily is recommended when taking Reduforte Biomed. Do not take more than 4 tablets per day. What side effects can Reduforte Biomed have? Reduforte Biomed has a good safety and tolerability rating s profile.Reduforte Biomed reduces the digestion of carbohydrates, which can cause bloating in some people during the first few days of use. However, this is not a cause for concern as the symptoms will disappear once your body adjusts to the increased amount of undigested carbohydrates.Side effects have only been observed in very rare cases ( What else needs to be considered? Keep in a dry place, at a maximum of 25°C and out of the reach of children.Use by: see instructions on the packaging.Do not take after the expiry date. What does Reduforte Biomed contain? 1 tablet contains:Main ingredient: Clavitanol? IQP VV 102, patented plant-derived complex.Excipients: microcrystalline cellulose, hydroxypropylmethylcellulose (HPMC), tricalcium phosphate, magnesium stearate.It contains no added preservatives, no artificial flavorings, no salt and no tieingredients. Where can you get Reduforte Biomed? Which packs are available? In pharmacies and drugstores without a doctor's prescription. Packs of 60 and 120 tablets. Distribution company Biomed AG, Überlandstrasse 199, 8600 Dübendorf. Manufacturer Chefaro Ireland DAC, The Sharp Building, Hogan Place, Dublin 2, Ireland. Status of Information April 2019...
93.38 USD
Resource instant protein ds 800g
Characteristics of Resource Instant Protein Ds 800 gAnatomical Therapeutic Chemical (АТС): V06DBStorage temp min/max 15/25 degrees CelsiusAmount in pack : 1 gWeight: 960g Length: 143mm Width: 143mm Height: 210mm Buy Resource Instant Protein Ds 800 g online from Switzerland..
110.92 USD
Schoenenberger plantain medicinal plant juice bottle 200 ml
Schönenberger ribwort juice is a naturally pure juice with ribwort from organic cultivation. The formulation has a supportive effect due to its cough-relieving properties. Natural juiceWith ribwortSoothes coughsFrom organic cultivationSuitable from 2 years of ageWithout preservatives Application Take 10 ml of Schönenberger ribwort juice diluted in water 3 to 4 times a day before meals. Note Shake well before useUse within 2 weeks after openingStore in the refrigerator after opening..
26.66 USD
Siccalix nasal ointment 20 g
What is Siccalix and when is it used? Siccalix is a nasal ointment for moistening dry nasal mucosa. Its promoting effects on the cell tissue support the regeneration of the skin and mucous membranes, especially in cases after an operation on the nasal septum. The two active ingredients contained in Siccalix, sea salt and dexpanthenol, complement each other in their effects. The properties of sea salt cause the nasal mucosa to be moistened, which means that the fine cilia in the nose are no longer obstructed and they can perform their function again. Dexpanthenol plays an important role in maintaining the metabolism in the upper cell layers of the skin and mucous membranes in the nose. Siccalix is used to moisten dry nasal mucosa, to clean the nasal cavities, to remove crusts. Upon recommendation pharmacist or on medical prescription, Siccalix is also used after operations on the nasal septum. When should Siccalix not be used? Siccalix should not be used if you are hypersensitive to one of the ingredients. When is caution required when using Siccalix? If used as directed, no special precautions need to be taken. Inform your doctor if you Pharmacist or druggist or your doctor if you• suffer from other diseases,• have allergies or• take other medicines (including those you bought yourself!) or use them externally!Can Siccalix be used during pregnancy or breastfeeding?During pregnancy and breastfeeding you should avoid taking medicines or consult a doctor as a precaution or ask your doctor for advice. How do you use Siccalix? Adults: Insert some ointment into both nostrils 2 - 3 times a day and then massage in gently. The use and safety of Siccalix nasal ointment in children and adolescents has not yet been 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, pharmacist or druggist.What side effects can Siccalix have?Siccalix has not had any side effects when used as directed.If you do notice any side effects, tell your doctor, pharmacist or druggist istin. What else should be observed? The medicinal product may only be used up to the date marked «EXP» on the container. Store at room temperature (15-25°C). Keep out of the reach of children. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Siccalix contain? 1 g Siccalix nasal ointment contains: Active ingredients: 10 mg sea salt, 50 mg dexpanthenol. Excipients: sorbitol, sodium methyl 4-hydroxybenzoate (E219), sorbic acid (E200), excip. per 1gAuthorization number47'880 SwissmedicWhere can you get Siccalix? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. One tube of Siccalix contains 20 g of nasal ointment. Authorization holder Drossapharm AG, 4002 Basel This leaflet was last checked by the drug authority (Swissmedic) in September 2007...
21.21 USD
Thick&easy neutral 225 g
Characteristics of Thick & Easy Neutral 225 gAnatomical Therapeutic Chemical (АТС): V06DXActive ingredient: V06DXAmount in pack : 1 gWeight: 299g Length: 101mm Width: 100mm Height: 120mm Buy Thick & Easy Neutral 225 g online from Switzerland..
37.04 USD
Venoruton forte tabl 500 mg 30 pcs
What is Venoruton forte and when is it used? Venoruton forte contains O-(β-hydroxyethyl)-rutoside, which contributes to the normalization of the function of the smallest blood vessels (capillaries) by increasing the resistance of their walls and reducing their permeability. In patients suffering from varicose veins or certain other leg vein conditions, these small vessels lose too much water, causing the ankles to swell.Venoruton forte brings relief by reducing this swelling and relieving the symptoms commonly associated with it, such as aching, tired or heavy legs and cramps. On the recommendation of a doctor, pharmacist or druggist, Venoruton forte can also be used to treat hemorrhoids. In the case of haemorrhoids, Venoruton forte causes rapid and sustained swelling of the mucous membrane of the anus and relieves symptoms such as pain, weeping, itching and bleeding. The preparation can also be used on the recommendation of a doctor in the event of side effects after radiation therapy and certain diseases of the retina (e.g. diabetic retinopathy). What should be considered? Um To relieve the symptoms of varicose veins, it is advisable to elevate your legs and raise the foot of the bed as much as possible during the day. Wearing elastic supports (usually stockings) is also recommended. When should Venoruton forte not be used? If you are sensitive to the active ingredient O-(β-hydroxyethyl)-rutoside, similar substances or an excipient, you should not use Venoruton forte. You must not take Venoruton forte during the first three months of pregnancy. Your doctor knows what to do in such cases.When should caution be taken when taking Venoruton forte?If the symptoms persist or if the symptoms worsen, a doctor must be consulted.If you have swollen legs due to heart, kidney or liver disease, you should not use Venoruton, as its effectiveness has not been tested in these patients.Use Venoruton is not recommended in children and adolescents.In rare cases, tiredness, dizziness and headaches have been reported after the use of Venoruton. If you feel dizzy or tired or have a headache, you should not drive or use machines.Inform your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies ortake or use external medicines (including those you bought yourself!)!Can Venoruton forte be taken during pregnancy or while breastfeeding? During pregnancy and breastfeeding, you should only take Venoruton forte after consulting your doctor. You must not take Venoruton forte during the first three months of pregnancy. Talk to your doctor if you are pregnant, planning to become pregnant or if you are breastfeeding.How do you use Venoruton forte?Adults:1 Venoruton forte tablet twice a day with meals. Relief of symptoms usually occurs within 2 weeks. The treatment can then be stopped (the improvement usually lasts for at least 4 weeks after stopping the preparation) and can be resumed as described above if the symptoms worsen again.Children and adolescents:The use and safety of Venoruton in children and adolescents has not yet been establishedbeen checked. Therefore, the use of Venoruton in children and adolescents is not recommended. Stick to the dosage given in the package leaflet or prescribed by your doctor. If you believe that the medicinal product is too weak or too strong, speak to your doctor, pharmacist or drugstore, pharmacist. In the case of radiation therapy or retina diseases. te side effects cause, but which do not have to occur with everyone. The side effects are mostly mild.Some patients may be allergic to this product and experience the following reactions: difficulty breathing or swallowing, swelling of the face, lips, tongue or throat, severe itching with a red rash, hives or hives. If you experience such reactions, you should stop the therapy and seek medical advice.The following side effects may occur when taking Venoruton:Rare (affects 1 to 10 users in 10,000): Gastrointestinal disturbances (including flatulence, diarrhoea, abdominal pain, stomach upset, indigestion) or itching.Very rare (affects less than 1 in 10' 000 people treated): dizziness, headache, tiredness, hot flushes. If you notice any side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered? Medicines should be kept out of the reach of children. Store at 15-30 °C, protected from moisture. The drug may only be used up to the date marked «EXP» on the container.Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed technical information.What does Venoruton forte contain?1 tablet contains 500 mg O-(β-hydroxyethyl)rutoside as an active ingredient and macrogol 6000 and magnesium stearate as auxiliary substances.Authorization number42647 (Swissmedic).Where can Venoruton forte be obtained? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Packs of 30 and 100 tablets. Authorization holder GSK Consumer Healthcare Schweiz AG, Risch. This leaflet was last checked by the drug authority (Swissmedic) in October 2015...
27.43 USD
Wala lens cristallina/viscum comp. cum stanno gtt opht 30 monodo
Characteristics of Wala crystalline lens / Viscum comp. cum stannous Gd Opht 30 Monodos 0.5 mlAnatomical Therapeutic Chemical (АТС): V03ZB03Amount in pack : 30 mlWeight: 60g Length: 45mm Width: 67mm Height: 77mm Buy Wala crystalline lens / Viscum comp. cum stannous Gd Opht 30 Monodos 0.5 ml online from Switzerland..
66.88 USD
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