Home NDC 82442-203 Tolnaftate
Product NDC 82442-203
11-digit product format 824420203
Labeler code 82442
Product ID 82442-203_5c1a026a-7ada-c393-e063-6394a90aa4a2
Type HUMAN OTC DRUG
Nonproprietary name Antifungal Liquid Spray
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Target Corporation
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-27
Substance TOLNAFTATE
Active strength 10 mg/g
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 Tolnaftate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 10 mg/g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82442-203-01 Tolnaftate 150 g in 1 CANISTER AEROSOL, SPRAY 150 2
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 Units Marketing start Sample Exclude flag Status 82442-203-01 82442020301 150 g in 1 CANISTER (82442-203-01) 150 g 2025-05-27 No No Current