Properties
What is it?
Composition 1g gel contains: Active substance: Diphenhydramine hydrochloride (INN Diphenhydramini hydrochloride) – 10mg. Excipients: Urea, Ethanol 96%, Trometamol, Lidocaine hydrochloride, Carbomer, Methylparahydroxybenzoate (E218), Purified water. Dosage form Gel for external use. Pharmacotherapeutic group: Antihistamine preparation for external use. ATC code: D04AA32 Pharmacological properties Dimedrol LMP, gel 10mg/g is an antihistamine preparation used for various types of itching. Diphenhydramine hydrochloride (Dimedrol) is a first-generation H1-histamine receptor blocker with pronounced antihistamine activity. Diphenhydramine hydrochloride reduces itching, swelling, and hyperemia. Diphenhydramine hydrochloride also has anti-allergic and local anesthetic effects. The excipient lidocaine hydrochloride is a local anesthetic that reduces accompanying itching and pain sensation. Indications Itching of skin and mucous membranes of various origins: allergic skin reactions, first-degree sun and thermal burns, insect bites, urticaria, eczema accompanied by itching, chickenpox. Contraindications Hypersensitivity to the active substances or other excipients. Do not use for itching of the eyes. The relationship between diphenhydramine and porphyria exacerbation has been established, therefore, it is not recommended for patients in this category to take the preparation. Special instructions Dimedrol LMP, gel 10mg/g is intended for external use only. After applying the gel, an occlusive dressing cannot be applied. Avoid getting the gel into the eyes, as the gel causes irritation. If this happens, wash your eyes with plenty of warm water. In children aged 2 months to 2 years, it is used under the supervision of medical personnel. In children with chickenpox, it can only be used with a doctor's permission. Pregnancy and lactation During pregnancy and lactation, it is used only after careful assessment of potential risk factors and consultation with a doctor. Effect of the preparation on the ability to drive vehicles and operate complex machinery The gel does not affect the ability to drive vehicles and operate complex machinery. Drug interactions No data on interactions are available. Overdose No information on overdose is available. Method of administration and dosage Apply the gel in a thin layer to the affected area and rub into the skin. The duration of use of the preparation is no more than 7 days. If prolonged use is necessary, consult a doctor. Side effects In some cases, skin irritation and sensitization (allergic) effects on the skin or mucous membranes (redness, inflammation) may occur. In such cases, discontinue the use of the gel. Report any side effects not listed in this instruction to your doctor or pharmacist! Dispensing rule: Pharmaceutical product group III, available without a prescription. Shelf life The shelf life is indicated on the packaging. Do not use after the expiry date! Storage Store in a place inaccessible to children. At a temperature not exceeding 25C. Protect from moisture. Store in a place protected from direct sunlight.