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Naftin Gel

Indications & Dosage
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INDICATIONS

Naftin® Gel, 1% is indicated for the topical treatment of tinea pedis, tinea cruris and tinea corporis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans* and Epidermophyton floccosum.*

*Efficacy for this organism in this organ system was studied in fewer than 10 infections.

DOSAGE AND ADMINISTRATION

A sufficient quantity of Naftin® Gel, 1% should be gently massaged into the affected and surrounding skin areas twice a day in the morning and evening. The hands should be washed after application. If no clinical improvement is seen after four weeks of treatment with Naftin® Gel, 1%, the patient should be re-evaluated.

HOW SUPPLIED

Naftin® (naftifine hydrochloride) 1% Gel is supplied in collapsible tubes in the following sizes:

20g - NDC 0259-4770-20
40g - NDC 0259-4770-40
60g - NDC 0259-4770-60

Note: Store at room temperature.

Manufactured for: Merz Pharmaceuticals, Greensboro, NC 27410. Rev 4/04. FDA rev date: 9/26/2007

Brand Name: Naftin Gel
Generic Name: Naftifine

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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