Storage:
active substance: naftifine;
1 ml of the drug contains 10 mg of naftifin hydrochloride;
excipients: ethanol 96%, propylene glycol, purified water.
Pharmaceutical form. Skin solution.
Main physico-chemical properties: transparent solution from colorless to light yellow color with the smell of ethanol.
Pharmacotherapeutic group.
Antifungal agents for use in dermatology.
ATX code D01A E22.
Indication.
Local treatment of fungal infections caused by naftifin sensitive pathogens:
– fungal infections of the skin and skin folds;
– interdigital mycoses;
– fungal nail infections;
– skin candidiasis;
– bran-like lichen;
– inflammatory dermatomycosis, accompanied or not accompanied by itching.
Contraindication.
Hypersensitivity to naftifin, propylene glycol or other components of the medicinal product. The drug cannot be applied to the wound surface. Do not use for eye treatment.
Method of application and dosage.
The drug should be applied to the affected skin surface and adjacent areas once a day after thorough cleaning and drying, covering approximately 1 cm of healthy skin around the edges of the affected area.
Duration of treatment: for dermatomycosis – 2-4 weeks (if necessary – up to 8 weeks); for candidiasis – 4 weeks; for nail infections – up to 6 months.
For fungal diseases of the nails, the drug is recommended to be used 2 times a day. Before the first application, it is necessary to remove the affected part of the nail as much as possible with scissors or a nail file (to facilitate this procedure, on the recommendation of the doctor, the nails can be treated with a special softening agent).
To prevent relapses, treatment with the drug should be continued for at least 2 weeks after the disappearance of the main symptoms of the disease.
Children. Data on the effectiveness and safety of the use of naftifin in children are insufficient, therefore it is not recommended to prescribe the drug to patients of this age category.
Overdose.
Acute overdose with local application of naftifin was not observed. Systemic intoxication with external use of the drug is unlikely due to the fact that a small amount of the active substance is absorbed through the skin.
In case of accidental ingestion of the solution, symptomatic treatment should be initiated.
Expiration date.
2 years from the date of production of the drug in bulk packaging.
Storage conditions.
Store in the original packaging at a temperature not higher than 25 °C.
Keep out of the reach of children.
Packaging. 20 ml of the drug in a bottle closed with a dropper stopper and closed with a lid, in a box.
Leave category. Without a prescription.
Producer. Limited liability company “Pharmaceutical firm “Vertex”.
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