United States · FDA National Drug Code directory

TOLNAFTATE ANTIFUNGAL

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
71335-2249_338b2c92-5505-4320-81d5-b5d3548f27e8
Product NDC
71335-2249
Form
POWDER
Composition / generic term
TOLNAFTATE
Labeler
Bryant Ranch Prepack
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20110801
Source listing expiry
20261231

Source-listed ingredients

  • TOLNAFTATE — 1 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 45 g in 1 BOTTLE, DISPENSING (71335-2249-1) · 71335-2249-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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