"Some cryogenic wart removers—which remove warts from the skin by freezing them off—have caught fire during use at home, harming consumers or setting fire to items around the house.
Since 2009, the Food and Drug Administratio"...
NAFTIN Gel is an allylamine antifungal indicated for the treatment of interdigital tinea pedis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum.
DOSAGE AND ADMINISTRATION
Apply a thin layer of NAFTIN Gel once daily to the affected areas plus an approximate ½ inch margin of healthy surrounding skin for 2 weeks.
For topical use only. NAFTIN Gel is not for ophthalmic, oral, or intravaginal use.
Dosage Forms And Strengths
Gel, 2%. Each gram contains 20 mg of naftifine hydrochloride in a colorless to yellow gel.
Storage And Handling
NAFTIN Gel is a colorless to yellow gel supplied in collapsible tubes in the following size:
45g – NDC 0259-1202-45
60g – NDC 0259-1202-60
Store NAFTIN Gel at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) [see USP Controlled Room Temperature].
NAFTIN (naftifine hydrochloride) Gel, 2% is manufactured for Merz Pharmaceuticals, LLC, Greensboro, NC 27410. Revised: October 2014.This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 10/27/2014
Additional Naftin Gel Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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