FDA label

What is naftifine used for?

The FDA-approved uses of naftifine, quoted from the Indications and Usage section of its DailyMed label.

Source: DailyMed SPL label file dated 2026-10-23. Publisher page

The FDA label says: “Naftifine Hydrochloride Cream USP, 1% is indicated for the topical treatment of tinea pedis, tinea cruris and tinea corporis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes,and Epidermophyton floccosum.”

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Naftifine Hydrochloride, cream

Indications and Usage, quoted from the label by Sun Pharmaceutical Industries, Inc. (ANDA205975). Cross-references to other label sections are left out.

Naftifine Hydrochloride Cream USP, 1% is indicated for the topical treatment of tinea pedis, tinea cruris and tinea corporis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes,and Epidermophyton floccosum.

Source: DailyMed label, set id d50961c2-e97f-4583-91d6-7cafd25a8c3d, version 3, effective July 7, 2025. NDC 51672-1362, one of 2 listings for this product.

Naftifine Hydrochloride, gel

Indications and Usage, quoted from the label by Sun Pharmaceutical Industries, Inc. (ANDA208201). Cross-references to other label sections are left out.

Naftifine hydrochloride gel USP, 2% is indicated for the treatment of interdigital tinea pedis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum.

Source: DailyMed label, set id 92d3ec30-2176-49cd-8a70-668ef65e7663, version 11, effective February 12, 2026. NDC 51672-1376, one of 1 listing for this product.

Questions

What is naftifine used for?

The FDA label says: “Naftifine Hydrochloride Cream USP, 1% is indicated for the topical treatment of tinea pedis, tinea cruris and tinea corporis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes,and Epidermophyton floccosum.”

What drug class is naftifine?

FDA lists naftifine in the Allylamine Antifungal established pharmacologic class.

Does this page cover off-label uses or dosing?

No. This page shows only the Indications and Usage section of the FDA label. Ask a pharmacist or prescriber about dosing.

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