Home NDC 83324-301 Maximum Strength Antifungal Liquid
Product NDC 83324-301
11-digit product format 833240301
Labeler code 83324
Product ID 83324-301_4f09ba13-b65c-fb78-e063-6294a90a7f64
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form LIQUID
Route TOPICAL
Labeler Chain Drug Marketing Association Inc
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-06-07
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 83324-301-01 Maximum Strength Antifungal Liquid 1 in 1 CARTON LIQUID 1 5 83324-301-01 Maximum Strength Antifungal Liquid 30 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83324-301 MAXIMUM STRENGTH ANTIFUNGAL LIQUID (TOLNAFTATE) LIQUID [CHAIN DRUG MARKETING ASSOCIATION INC] 2 Current NDC, 2 package rows 20241213_1a4f4d10-6782-ddb4-e063-6294a90ac206.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 83324-301-01 83324030101 1 BOTTLE, WITH APPLICATOR in 1 CARTON (83324-301-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR 2024-06-07 No No Current