Wounds and ulcers treatment
(1 Pages)
Bepanthen sensiderm cream tb 50 g
Characteristics of Bepanthen Sensiderm cream Tb 50 gAnatomical Therapeutic Chemical (АТС): D03AX03Certified in Europe CEAmount in pack : 1 gWeight: 68g Length: 26mm Width: 150mm Height: 37mm Buy Bepanthen Sensiderm cream Tb 50 g online from Switzerland..
46.25 USD
Biafine emuls tb 186g
What is Biafine and when is it used? Biafine is an emulsion that is applied to the skin to treat small, first-degree skin burns, minor wounds and non-infected injuries such as abrasions or ulcers (sores) of the legs, and to protect and heal sensitive skin.With a doctor's prescription, Biafine can be used alternately with other dermatological medicines containing active ingredients .What should be considered?Biafine is not a care or sun protection cream. It should not be used in the area of the mucous membranes or near the eyes. In the case of extensive burns, you must consult your doctor. Large, heavily soiled and deep wounds, as well as wounds from bites or stings, must be treated by a doctor (risk of tetanus). If the extent of an injury does not decrease after a certain time or if the wound heals within If it does not improve after a week, it is advisable to see a doctor. This is also the case if the edges of the wound are very red, if the wound suddenly swells, is very painful or is accompanied by fever (risk of infection).When must Biafine not be used?Biafine must not be used if you are allergic to any of the ingredients (see «What does Biafine contain?»). It should also not be applied to wounds that are infected or bleeding profusely.When should caution be taken when using Biafine?Biafine should not be used 3 hours before radiotherapy. Avoid using this emulsion for a long time and on large areas without first talking to your doctor, pharmacist or druggist. The use and safety of Biafine Emulsion in children and adolescents have not been studied to date. This medicinal product contains 23 mg propylene glycol per g of cream. Propylene glycol may cause skin irritation. This medicinal product contains 1 mg of benzoate per g of cream, as sodium methyl p-hydroxybenzoate (E 219) and sodium propyl p-hydroxybenzoate (E 217) and may cause allergic reactions, including delayed reactions. Contains potassium sorbate (E 202): May cause localized skin irritation (e.g. contact dermatitis). This medicinal product contains a Fragrance with 3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one, benzyl benzoate, citral, citronellol, D-limonene, eugenol, geraniol, 2-benzylideneoctanal, hydroxycitronellal, hydroxymethylpentyl-cyclohexenecarboxaldehyde, isoeugenol and linalool. 3-Methyl-4-(2,6, 6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one, benzyl benzoate, citral, citronellol, D-limonene, eugenol, geraniol, 2-benzylideneoctanal, hydroxycitronellal, hydroxymethylpentyl-cyclohexenecarboxaldehyde, isoeugenol and linalool can cause allergic reactions.Inform your doctor, pharmacist or druggist , pharmacist or druggist, if yousuffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Biafine be used during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the 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 Biafine?AdultsFirst degree burnsApply a thick layer until the skin can no longer absorb the emulsion. Allow the emulsion to soak in by gently massaging it in. Repeat 2 to 4 times a day.Skin injuriesAfter cleaning the wound, apply a thick layer of emulsion well beyond the edges of the wound. Repeat the application regularly so that the wound is generously covered with Biafine the whole time. Cover with a damp compress if necessary. Do not use absorbent bandages. Protection and healing of sensitive skin Massage gently 2 to 3 times a day at regular intervals The use and safety of Biafine in children and adolescents has not yet been tested. Respect 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 Biafine have?Uncommon (affects 1 to 10 users in 1000) transient moderate pain like a tingling sensation has been observed after using Biafine.Very rarely (affects less than Local skin reactions (including local hypersensitivity reactions such as mild skin changes, swelling, rashes or redness) have been reported in approximately 1 in 10,000 users.If hypersensitivity reactions occur (itching, severe burning, skin rash), please tell your doctor and stop treatment.If you notice any side effects, contact your doctor, pharmacist or druggist 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 date marked «EXP» on the container.Storage instructionsStore at room temperature (15-25°C). Do not store in the freezer.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 Biafine contain?Active substancesNone.1 g oil in water emulsion contains approx. 6% (m/m) fat.ExcipientsTrolamine; ethylene glycol monopalmitostearates; stearic acid; cetyl palmitate; hard paraffin; thin liquid paraffin; squalane; avocado oil; propylene glycol (E1520); trolamine and sodium alginate; potassium sorbate (E202); sodium methyl p-hydroxybenzoate (E219); sodium methyl p-hydroxybenzoate (E217); Aroma (contains 3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one, benzyl benzoate, citral, citronellol, D-limonene, eugenol, geraniol, 2-benzylideneoctanal, hydroxycitronellal, hydroxymethylpentyl-cyclohexenecarboxaldehyde, isoeugenol and linalool); purified water.Approval number55470 (Swissmedic)Where can you get Biafine? Which packs are available? In pharmacies and drugstores, without a doctor's prescription. Tubes of 93 g and 186 g. Authorization holder Janssen-Cilag AG, Zug, ZG This package leaflet was last checked by the drug authority (Swissmedic) in June 2020. ..
46.36 USD
Hametum ointment tb 100 g
Hametum contains active herbal ingredients from Hamamelis virginiana, the Virginian witch hazel. Hametum has anti-inflammatory, astringent and local hemostatic properties. It promotes the healing of minor skin injuries, relieves itching and has a cooling and pain-relieving effect. Hametum is used for the treatment of minor skin injuries such as abrasions and cuts, cracked, chapped skin, local irritation of the skin and mucous membranes, dry and sore nasal mucosa, Hemorrhoids, against soreness in children, adolescents and adults, wolf, for burn blisters and sunburn of a lighter degree. Swissmedic-approved patient informationHametum® ointmentSchwabe Pharma AGHerbal medicinal product What is Hametum and when is it used?Hametum contains active herbal ingredients from Hamamelis virginiana, the Virginian witch hazel. Hametum has anti-inflammatory, astringent and local hemostatic properties. It promotes the healing of minor skin injuries, relieves itching and has a cooling and pain-relieving effect. Hametum is used for the treatment of minor skin injuries such as abrasions and cuts, cracked, chapped skin, local irritation of the skin and mucous membranes, dry and sore nasal mucosa, Hemorrhoids, against soreness in children, adolescents and adults, wolf, for burn blisters and sunburn of a lighter degree. When should Hametum not be used or only with caution?Use in children under the age of 2 is not recommended as there is insufficient data for this age group. If a local deterioration occurs or if healing does not occur within 2-3 weeks, a doctor, pharmacist or druggist should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. If you are hypersensitive to one of the ingredients, such as wool wax or cetostearyl alcohol, the ointment must not be used. May cause localized skin irritation (e.g. contact dermatitis). This medicinal product contains 8.3 mg propylene glycol per 0.5 cm strand of ointment, equivalent to 50 mg/g ointment. Tell your doctor, pharmacist or druggist if you suffer from other illnesses,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Hametum be used during pregnancy or breastfeeding?Based on previous experience, there is no known risk for the child when 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 Hametum?Adults, adolescents and children from 2 years of age: Unless otherwise prescribed, apply a thin layer of Hametum several times a day or massage in lightly as required. A strand of ointment 0.5 cm long corresponds to 0.17 g of ointment. For local treatment of hemorrhoids, insert ointment twice a day using a screw-on cannula (25 g, 35 g and 50 g tubes with cannula). Stick to the dosage given in the package insert or prescribed by your doctor. If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist. The use and safety of Hametum ointment in children under 2 years of age has not yet been tested. This medicinal product contains 8.3 mg propylene glycol per 0.5 cm strand of ointment, equivalent to 50 mg/g ointment. What side effects can Hametum have?Up to now, no side effects have been observed for Hametum when used as intended. If you nevertheless observe side effects, inform your doctor, pharmacist or druggist. If allergic reactions occur again (e.g. skin reddening, itching), you should refrain from further use and, if necessary, inform a doctor. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Storage instructionsStore at room temperature (15-25°C). Keep out of the reach of children. Further informationDo not ingest. Your doctor, pharmacist or druggist can provide you with further information. What does Hametum contain?1 g of ointment contains: Active ingredients62.5 mg distillate from fresh leaves and twigs of Hamamelis virginiana (Hamamelis virginiana L., folium et ramus recens), Drug-distillate ratio 1:1.12-2.08, distillation agent: ethanol 7.5% v/v ExcipientsWhite vaseline, wool wax 165.0 mg, glycerol (mono/di/tri) (adipate, alkanoate(C6- C20)), isostearate, cetylstearyl alcohol 20.0 mg, microcrystalline wax, citric acid glycerol monooleate glycerol monostearate-L-(+)-6-0-palmitoylascorbic acid-DL-alpha-tocopherol lecithin (2 ,5:7,5:20:20:25:25), Propylene Glycol 50mg, Purified Water, Edetate Sodium, Liquid ParaffinApproval number08653 (Swissmedic) Where can you get Hametum? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Packs of 25 g, 35 g and 50 g with needle and packs of 50 g and 100 g without needle. Authorization holderSchwabe Pharma AG, Erlistrasse 2, 6403 Küssnacht am Rigi. This leaflet was last checked by the Medicines Agency (Swissmedic) in November 2020. ..
50.21 USD
Ialugen cream tb 60 g
ialugen contains sodium hyaluronate as an active ingredient, a natural substance that accelerates scarring. ialugen is available as a cream and medicated gauzes. It is a wound healing agent that accelerates the healing of small, minor wounds and minor burns (1st degree). ialugen can only be used to treat ulcers if prescribed by a doctor. Swissmedic-approved patient informationialugen®IBSA Institut Biochimique SAWhat is ialugen and when is it used?ialugen contains sodium hyaluronate as an active ingredient, a natural substance that accelerates scarring. ialugen is available as a cream and medicated gauzes. It is a wound healing agent that accelerates the healing of small, minor wounds and minor burns (1st degree). ialugen can only be used to treat ulcers if prescribed by a doctor. What should be considered?Large, heavily contaminated or deep wounds, such as bite and puncture wounds, require medical treatment (danger of tetanus). If the wound size does not decrease within a certain time or if the wound has not healed after 10-14 days, you should also consult the doctor. You should do the same if the edges of the wound are very red, if the wound suddenly swells and becomes very painful, or if you have a fever (risk of blood poisoning). When not to use ialugen?You should not use ialugen cream and gauze if you are allergic to one or more of the ingredients (see «What is in ialugen contain?») are allergic. The same limitation applies to severe, deep and heavily contaminated wounds. Such injuries must be cleaned under medical supervision. When should you be careful when using ialugen?In very rare cases, sodium hyaluronate or any additives contained in ialugen, especially if used for a long time, can allergic symptoms (e.g. itching) (see «What side effects can ialugen have?»). In such cases, it is recommended to interrupt therapy and inform your doctor. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally.Can ilugen 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 not 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 ialugen?Before applying ialugen cream and gauze, the wounds and their surroundings must be cleaned and disinfected. In particular, it is recommended to remove the cream residues from a previous application. Cream: Unless otherwise prescribed by the doctor, the ialugen cream is applied 2-3 times a day in a thin layer evenly over the entire injury until the scar has formed. The cream is easy to wash off with water. Medicated gauze: Depending on the wound surface, apply one or more gauzes 2 or more times a day. The ialugen gauze must be removed with sterile forceps and placed on the previously cleaned and disinfected wound; then cover the wound with a sterile gauze and then with cotton wool and fix the whole thing with a suitable bandage. The individual packs are intended for single use. The use and safety of ialugen in children and adolescents has not yet been tested. Based on previous experience, there is no known risk for the child when used as intended. 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, pharmacist or druggist. What side effects can ialugen have?The following side effects can occur when using ialugen: In very rare cases, sodium hyaluronate or any additives contained in ialugen can lead to allergic symptoms (e.g. itching, eczema, reddening of the skin, skin reactions or burning sensation), especially after long-term use. In such cases, it is recommended to interrupt therapy and inform your doctor. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Shelf lifeThe medicinal product may only be used up to the date marked on the container with « EXP» can be used. Use by after openingOnce opened, the 500g dispenser can be used within 6 months. Storage instructionsStore at room temperature (15 - 25°C) and keep out of the reach of children. Further informationDo not use if the expiry date has passed, but return to the pharmacy for disposal. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does ialugen contain?Active ingredientsSodium hyaluronate, 2 mg per 1 g cream, or 2 mg per 4 g of medicated gauze (0.5 mg per 1 g of gauze). ExcipientsCream: sodium laurilsulfate, preservatives: sorbic acid (E200), propyl parahydroxybenzoate (E216), methyl parahydroxybenzoate (E218) and other excipients. Gazen: Auxiliaries for the preparation of an ointment Approval number48118, 48119 (Swissmedic) Where do you get ialugen? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Cream: Tubes of 20 g, 25 g and 60 g (GB) Medicated gauzes: packs of 10 and 30 gauzes (individually wrapped) (D). Authorization holderIBSA Institut Biochimique SA, Lugano This leaflet was last checked by the Medicines Agency (Swissmedic) in November 2021. ..
56.48 USD
Ialugen medical gauze 10x10cm 10 pcs
ialugen contains sodium hyaluronate as an active ingredient, a natural substance that accelerates scarring. ialugen is available as a cream and medicated gauzes. It is a wound healing agent that accelerates the healing of small, minor wounds and minor burns (1st degree). ialugen can only be used to treat ulcers if prescribed by a doctor. Swissmedic-approved patient informationialugen®IBSA Institut Biochimique SAWhat is ialugen and when is it used?ialugen contains sodium hyaluronate as an active ingredient, a natural substance that accelerates scarring. ialugen is available as a cream and medicated gauzes. It is a wound healing agent that accelerates the healing of small, minor wounds and minor burns (1st degree). ialugen can only be used to treat ulcers if prescribed by a doctor. What should be considered?Large, heavily contaminated or deep wounds, such as bite and puncture wounds, require medical treatment (danger of tetanus). If the wound size does not decrease within a certain time or if the wound has not healed after 10-14 days, you should also consult the doctor. You should do the same if the edges of the wound are very red, if the wound suddenly swells and becomes very painful, or if you have a fever (risk of blood poisoning). When not to use ialugen?You should not use ialugen cream and gauze if you are allergic to one or more of the ingredients (see «What is in ialugen contain?») are allergic. The same limitation applies to severe, deep and heavily contaminated wounds. Such injuries must be cleaned under medical supervision. When should you be careful when using ialugen?In very rare cases, sodium hyaluronate or any additives contained in ialugen, especially if used for a long time, can allergic symptoms (e.g. itching) (see «What side effects can ialugen have?»). In such cases, it is recommended to interrupt therapy and inform your doctor. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally.Can ilugen 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 not 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 ialugen?Before applying ialugen cream and gauze, the wounds and their surroundings must be cleaned and disinfected. In particular, it is recommended to remove the cream residues from a previous application. Cream: Unless otherwise prescribed by the doctor, the ialugen cream is applied 2-3 times a day in a thin layer evenly over the entire injury until the scar has formed. The cream is easy to wash off with water. Medicated gauze: Depending on the wound surface, apply one or more gauzes 2 or more times a day. The ialugen gauze must be removed with sterile forceps and placed on the previously cleaned and disinfected wound; then cover the wound with a sterile gauze and then with cotton wool and fix the whole thing with a suitable bandage. The individual packs are intended for single use. The use and safety of ialugen in children and adolescents has not yet been tested. Based on previous experience, there is no known risk for the child when used as intended. 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, pharmacist or druggist. What side effects can ialugen have?The following side effects can occur when using ialugen: In very rare cases, sodium hyaluronate or any additives contained in ialugen can lead to allergic symptoms (e.g. itching, eczema, reddening of the skin, skin reactions or burning sensation), especially after long-term use. In such cases, it is recommended to interrupt therapy and inform your doctor. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Shelf lifeThe medicinal product may only be used up to the date marked on the container with « EXP» can be used. Use by after openingOnce opened, the 500g dispenser can be used within 6 months. Storage instructionsStore at room temperature (15 - 25°C) and keep out of the reach of children. Further informationDo not use if the expiry date has passed, but return to the pharmacy for disposal. Your doctor, pharmacist or druggist can provide you with further information. These people have the detailed information for specialists. What does ialugen contain?Active ingredientsSodium hyaluronate, 2 mg per 1 g cream, or 2 mg per 4 g of medicated gauze (0.5 mg per 1 g of gauze). ExcipientsCream: sodium laurilsulfate, preservatives: sorbic acid (E200), propyl parahydroxybenzoate (E216), methyl parahydroxybenzoate (E218) and other excipients. Gazen: Auxiliaries for the preparation of an ointment Approval number48118, 48119 (Swissmedic) Where do you get ialugen? What packs are available?In pharmacies and drugstores, without a doctor's prescription. Cream: Tubes of 20 g, 25 g and 60 g (GB) Medicated gauzes: packs of 10 and 30 gauzes (individually wrapped) (D). Authorization holderIBSA Institut Biochimique SA, Lugano This leaflet was last checked by the Medicines Agency (Swissmedic) in November 2021. ..
39.62 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
Peru stick twist pen 21 g
Peru-Stick is a balm stick that should be rubbed into the areas to be treated for skin tears, abrasions, slight cuts and chilblains. It is believed that Peru stick forms a protective film and can thus relieve the accompanying pain. Swissmedic-approved patient informationPeru-StickTentan AGAMZVWhat is Peru-Stick and when is it used ? Peru-Stick is a balm stick that should be rubbed into the areas to be treated in the event of skin tears, abrasions, slight cuts or chilblains. It is believed that Peru stick forms a protective film and can thus relieve the accompanying pain. What should be considered?If a local deterioration occurs or if healing does not take place within 2-3 weeks, a doctor should be consulted. When should Peru-Stick not be used?Peru-Stick should not be used if you are hypersensitive to any of the ingredients. Peru-Stick must not be used on skin tears or cracks in the mammary glands while breastfeeding (see under «Can Peru-Stick be used during pregnancy or while breastfeeding?»). Peru-Stick should not be used in children under 12 years of age. When is caution required when using Peru Stick? Peru-Stick is only intended for external use on the skin. Avoid contact with eyes or mucous membranes. Do not use on large areas (10% of the body surface) or over a long period of time. There is a risk of developing an allergy to Balsam of Peru, so long-term use on broken skin is not recommended. As a precautionary measure and to reduce this risk, it is advisable to only use the Peru Stick until the injured skin has healed (see under «What side effects can Peru Stick have?»). This medicine also contains wool wax (lanolin). Wool wax can cause localized skin irritation (e.g. contact dermatitis). Do not ingest. In the event of accidental ingestion, a doctor must be consulted immediately. Tell your doctor, pharmacist or druggist if you suffer from other diseases,have allergies ortake other medicines (including those you bought yourself!) or use them externally!Can Peru-Stick be used during pregnancy or breastfeeding?PregnancySystematic scientific studies have not been carried out . There are also no controlled studies of use in pregnant women. Peru Stick must not be used during pregnancy. BreastfeedingIt is not known whether the active ingredients are excreted in breast milk. As a precaution, use during breast-feeding is not recommended. Peru Stick must not be used on skin tears or cracks in the mammary glands. How do you use Peru Stick?Adults and adolescents aged 12 and over: Unless otherwise prescribed by the doctor, apply to the affected areas twice a day. Because of the risk of developing an allergy to Peru balsam, long-term use on broken skin is not recommended (see «What side effects can Peru stick have?»). The use and safety in children under 12 years of age 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, pharmacist or druggist. What side effects can Peru Stick have?The following side effects can occur when using Peru Stick: In rare cases, hypersensitivity reactions and local skin reactions that manifest as itching, burning or redness. In this case, the application should be discontinued and a doctor consulted if necessary. In rare cases, especially with long-term use, an allergy to balsam of Peru may develop, which makes it necessary to discontinue the preparation. Symptoms of an overdose after accidental or intentional ingestion or extensive or prolonged use of Peru-Stick can include nausea, vomiting, abdominal cramps and disorders of the central nervous system. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?The medicinal product may only be used up to the date marked «EXP» on the container. Store medicines out of the reach of children. Store at room temperature (15-25°C). Your doctor, pharmacist or druggist can provide you with further information. What is in Peru Stick?1g Peru Stick contains: Active ingredients: Lidocaine 12.17 mg, Peru balsam 4.86 mg, dextrocamphor 4.86 mg, native castor oil 4.86 mg. Excipients: yellow wax, thin paraffin, hard paraffin, wool wax (lanolin), white vaseline, wool wax alcohols, geranium oil, hard fat. Approval number 14809 (Swissmedic). Where can you get Peru Stick? What packs are available?In pharmacies and drugstores without a doctor's prescription. Twisting pin at 21 g Authorization holderTentan AG, 4452 Itingen. This leaflet was last checked by the Medicines Agency (Swissmedic) in August 2018. PI059000/02.19 ..
22.41 USD
Unguentolan ointment tb 50 g
What is Unguentolan and when is it used? Unguentolan promotes wound healing and regeneration of injured tissue. Unguentolan can be used for small superficial injuries, skin damage and minor burns (1st degree) (also for sunburn and cold injuries). Unguentolan may only be used on children under 2 years of age if prescribed by a doctor. What should be considered? Large, heavily soiled and deep wounds, as well as bite and puncture wounds require medical treatment (danger of tetanus). If the size of a wound remains unchanged for some time or if the wound does not heal within 10-14 days, a doctor's visit is also necessary. The same applies if the edges of the wound are very red, the wound suddenly swells, is very painful or the injury is accompanied by fever (danger of blood poisoning). See also «When should Unguentolan not be used?». When should Unguentolan not be used? Unguentolan should not be used if there is a known intolerance to the active ingredient cod liver oil or one of the excipients according to the composition (e.g. the preservative). If there is a risk of infection (e.g. extensive burns, inflamed wounds, heavily soiled wounds, deep wounds, bite wounds, Puncture wounds) Unguentolan must not be used. There is a risk of blood poisoning or a possible complication of tetanus.When should you be careful when using Unguentolan?See a doctor if you have suffered an injury with a risk of infection, such as extensive burns, inflamed wounds, deep wounds, bite or puncture wounds or heavily soiled wounds. The doctor will decide on the necessary treatment. If the size of a wound remains unchanged for some time or if the wound does not heal within 10-14 days, treatment with Unguentolan wound ointment should be discontinued and a doctor consulted. This also applies if there are signs of infection, e.g. the edges of the wound are very red, the wound suddenly swells, is very painful or the injury is accompanied by fever.In the case of X-ray radiation, it should be noted that Unguentolan may increase the irritation and reddening of the skin.Unguentolan must not come into contact with the mucous membranes and especially not with the eyes.Be particularly careful when using Unguentolan is required if you want to expose yourself to UV light (e.g. sun, sunlamps, solariums) during use.Butylhydroxytoluene can cause localized skin irritation (e.g. contact dermatitis), irritation of the eyes and mucous membranes.Propyl parahydroxybenzoate (E216) can cause allergic reactions, including delayed reactions.Unguentolan should not be used during pregnancy.If should it be necessary to use it while breastfeeding, you must not use Unguentolan in the chest area in order to avoid direct contact between the infant and the active ingredient. See «Can Unguentolan be used during pregnancy or while breastfeeding?»Inform your doctor, pharmacist or druggist if yousuffer from other diseases,have allergies ortake or use external medicines (including those you bought yourself!).May Can Unguentolan be used during pregnancy or while breastfeeding?PregnancySystematic scientific studies on use during pregnancy have not been carried outperformed. Vitamin A can enter the bloodstream through the skin, but to what extent is not known. Therefore, Unguentolan should not be used during pregnancy.Breastfeeding If it is necessary to use Unguentolan while breastfeeding, you must not use Unguentolan in the breast area to avoid direct contact between the infant and the active ingredient. How do you use Unguentolan? Clean the skin areas or wounds to be treated as well as possible before use. Apply Unguentolan and apply a bandage if necessary. If a bandage is used, it is recommended to change the bandage once a day. 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, pharmacist or druggist.What side effects can Unguentolan have?Intolerance reactions (allergies) are very rare. If you experience skin reactions such as itching, severe burning or a rash, please inform your doctor, pharmacist or druggist.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 .Do not ingest. Store at room temperature (15–25 °C). The medicine may only be used up to the date marked «EXP» on the container. Your doctor, pharmacist or druggist can provide you with further information. What does Unguentolan contain? 1 g ointment contains: Active ingredients: 100 mg cod liver oil , 79 μg retinol acetate corresponds to 385 IU vitamin A. Flavouring: ethyl vanillin. Antioxidant: butylated hydroxyanisole (E 320). Preservative: propyl paraben (E 216) and other excipients. Authorization number 13188 (Swissmedic)Where can you get Unguentolan? Which packs are available? In pharmacies and drugstores without a doctor's prescription. Tubes of 50 and 100 g. Authorization holder Gebro Pharma AG, 4410 Liestal This leaflet was last checked by the drug authority (Swissmedic) in July 2019....
22.92 USD
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