Home NDC 79481-0660 Maximum Strength Antifungal Liquid
Product NDC 79481-0660
11-digit product format 794810660
Labeler code 79481
Product ID 79481-0660_57c6ebd5-bf13-3371-e063-6394a90a91a0
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form LIQUID
Route TOPICAL
Labeler Meijer Distribution Inc
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-29
Substance TOLNAFTATE
Active strength 10 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Maximum Strength Antifungal Liquid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 06KB629TKV Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313423 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79481-0660-1 Maximum Strength Antifungal Liquid 1 in 1 CARTON LIQUID 1 4 79481-0660-1 Maximum Strength Antifungal Liquid 30 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79481-0660 MAXIMUM STRENGTH ANTIFUNGAL LIQUID (TOLNAFTATE) LIQUID [MEIJER DISTRIBUTION INC] 3 Current NDC, 2 package rows 20241016_0b3eb169-b309-8c1a-e063-6294a90a726e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 49 · 973 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 79481-0660-1 79481066001 1 BOTTLE, WITH APPLICATOR in 1 CARTON (79481-0660-1) / 30 mL in 1 BOTTLE, WITH APPLICATOR 2026-07-29 No No Current