Ulcer treatment
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Bepanthen ointment 5% tb 30 g
Bepanthen MED ointment contains the active ingredient dexpanthenol, which is incorporated into an ointment base with a high fat content. The active ingredient dexpanthenol is converted into the vitamin pantothenic acid in the skin and supports the structure and regeneration of the skin from the inside out. The high fat content of Bepanthen MED ointment forms a fine lipid film on the skin's surface and protects it from external influences and moisture loss. Bepanthen MED ointment is used in baby care for the treatment and prevention of diaper infections, for breast care during breastfeeding and for the treatment of sore nipples, breast fissures, for the prevention and treatment of sore and cracked skin, for dry skin, to support wound healing and the Epithelialization (formation of skin cells) in minor injuries, banal burns and abrasions, skin irritations, for example after UV light and light therapy, chronic ulcers (ulcers), bedsores (bed sores), fissures (skin and mucous membrane tears), skin transplants, cervical erosions (defects the mucous membrane of the cervix) and in interval treatments after cortisone therapy. Swissmedic-approved patient informationBepanthen® MED ointmentBayer (Schweiz) AGWhat is Bepanthen MED ointment and when is it used?..
17.32 USD
Kamillosan cream tb 40 g
Kamillosan Crème contains an active component of chamomile, the essential oil, in quantified amounts. Kamillosan Cream serves as an anti-inflammatory, analgesic, antipruritic, astringent, slightly disinfectant with calming and odor-eliminating properties. Kamillosan Crème can be used for minor skin injuries such as abrasions, scratches, cracked skin and burn blisters. Swissmedic-approved patient informationKamillosan® Cream, CreamMEDA Pharma GmbHHerbal medicinal product What is in Kamillosan Crème and when is it used?Kamillosan Crème contains an active component of chamomile, the essential oil, in a quantified amount. Kamillosan Cream serves as an anti-inflammatory, analgesic, antipruritic, astringent, slightly disinfectant with calming and odor-eliminating properties. Kamillosan Crème can be used for minor skin injuries such as abrasions, scratches, cracked skin and burn blisters. What should be considered?If local deterioration occurs or if healing does not take place within 2-3 weeks, a doctor should be consulted. If the general condition deteriorates (e.g. fever), a doctor must be consulted immediately. When should Kamillosan Crème not be used or only with caution?Kamillosan Crème should not be used if there is a known hypersensitivity to one of the ingredients. Hypersensitivity to other daisy family (Asteraceae) such as Achillea millefolilum (sheep gift), Arnica montana (arnica), mugwort, Bellis perennis (daisy), Calendula officinalis (marigold), chrysanthemum, echinacea (coneflower) can lead to allergic cross-reactions (see «What side effects can Kamillosan Cream have?»). The use and safety of Kamillosan Crème has not yet been tested in children and adolescents. Therefore, the application is not recommended. Before breastfeeding newborns, the mother must remove the cream around her nipples. Kamillosan Crème contains cetostearyl alcohol and wool wax alcohols, which can cause local skin reactions (e.g. contact dermatitis), as well as methyl 4-hydroxybenzoate and propyl 4-hydroxybenzoate (parabens E 218 and E 216), which can trigger allergic reactions (also delayed reactions). . Inform your doctor, pharmacist or druggist if you suffer from other illnesses, have allergies or are taking other medicines (even those you bought yourself!) or using them externally! How do you use Kamillosan Crème?For adults, Kamillosan Crème should initially be applied thinly to the affected skin areas about 3 times a day. As soon as the clinical picture improves, 2 applications a day are sufficient. The use and safety of Kamillosan, cream has not yet been tested in children and adolescents. 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 Kamillosan Cream have? Painful, itchy and inflammatory skin changes. The following side effects can be observed with an unknown frequency: Hypersensitivity reactions to chamomile (e.g. contact dermatitis)Cross-reactions (allergic reactions) in people with hypersensitivity to other daisy family such as arnica, mugwort, daisies, marigolds, coneflowers, chrysanthemums, daisies or hypersensitivity to the ingredients of the cream base (see also «When should Kamillosan Cream not be used or should only be used with caution?») Severe allergic reactions with shortness of breath, facial swelling, circulatory collapse and anaphylactic shock after contact with mucous membranes, especially in cases of improper use of liquid chamomile preparations.Methyl 4-hydroxybenzoate and propyl -4-Hydroxybenzoate (parabens E 218 and E 216) can cause allergic reactions, including delayed reactionsIn these cases, treatment should be discontinued and a doctor consulted if necessary. If you notice side effects that are not described here, you should inform your doctor, pharmacist or druggist. What else needs to be considered?Store at room temperature (15-25 °C) and out of the reach of children. Use by period after opening: 12 months. The medicinal product may only be used up to the date marked “EXP” on the package. Your doctor, pharmacist or druggist can provide you with further information. What does Kamillosan Cream contain?1 g Kamillosan Cream contains 20 mg ethanolic extract from chamomile flowers (drug-extract ratio: 2.7 - 5.5: 1; extraction agent 95.4% ethanol [v/v]) corresponding to a minimum content of 0.2 mg essential oil, of which 0.07 mg levomenol ([-]-α-bisabolol). This preparation also contains wool wax alcohols; Preservatives: methyl p-hydroxybenzoate (E218), propyl p-hydroxybenzoate (E216) and other additives. Approval number46180 (Swissmedic). Where can you get Kamillosan Cream? What packs are available? Kamillosan Crème is available in pharmacies and drugstores without a doctor's prescription. Packs of 40 g are available. Authorization holderMEDA Pharma GmbH, 8602 Wangen-Brüttisellen. This leaflet was last checked by the drug authority (Swissmedic) in September 2018. ..
26.76 USD
Unguentolan ointment tb 100 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. ..
28.07 USD
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