WARNINGS The medicine is for external use only. The use, especially if prolonged, of the product can give rise to sensitization phenomena. The efficacy and safety of benzocaine depend on a correct dosage. Therefore it is necessary to use the minimum quantity of product sufficient to obtain the desired effect, applying it with caution in subjects with severely damaged mucous membranes and site of inflammatory processes that could cause excessive absorption of this active ingredient. It should only be used on non-extensive and superficial skin lesions and for short periods of time. Do not apply near the eyes. In case of deep wounds, or disseminated insect bites, or severe burns, or particularly extensive minor burns, always consult your doctor before using the product. If the morbid condition for which this preparation is used persists longer, if irritation occurs, if redness, swelling or pain persists or if you have an infection, discontinue use and consult your doctor. Do not use the product in children younger 'less than 6 months; administration is recommended only after consulting your doctor between 6 months and 2 years of age. PHARMACOTHERAPEUTIC CATEGORY Dermatological - local anesthetics. STORAGE No particular precautions. CONTRAINDICATIONS / SECONDARY EFFECT Hypersensitivity 'to the active ingredients or to any of the excipients. The product is not suitable for ophthalmic use. NAME FOILLE BURNS EXCIPIENTS Hydrogenated vegetable oil, ceresin (solid paraffin), yellow beeswax, monodiglycerides (of higher fatty acids), corn oil, calcium hydrate, sodium borate, PEG 32, sodium lauryl sulfate, maleic anhydride, eugenol, sodium calcium EDTA, 8 -hydroxyquinoline, purified water. SIDE EFFECTS The use of products for topical application, especially if prolonged, can give rise to sensitization phenomena. In this case, stop the treatment and institute a suitable therapy. Rarely, a high absorption of benzocaine can cause serious reactions (increased methemoglobin, with the appearance of cyanosis), particularly in children and the elderly, which require prompt hospital intervention. PREGNANCY AND BREASTFEEDING There are no known contraindications for use in case of pregnancy or breastfeeding. However, it is advisable to consult your doctor before taking the drug during pregnancy and breastfeeding. INDICATIONS Minor burns, sun rashes, skin irritations from various chemical-physical agents, insect bites. In the dressing of abrasions, abrasions and superficial wounds of the skin. INTERACTIONS None known. DOSAGE Apply the cream in a thin and uniform layer directly on the lesion. In case of limited lesions, it is advisable, after applying the cream, to cover with sterile gauze. The dressing should not be removed for at least 48 hours in order not to disturb the granulation process. In some cases the initial dressing will not have to be removed and changed even for a longer period of time, but must gradually keep it well moistened with the product. It is recommended not to exceed the maximum limit of 4 applications per day, in both adults and children. ACTIVE PRINCIPLES 100 g of cream contains 4 g of benzyl alcohol, 5 g of benzocaine 0,10 g of chloroxylenol.