Home NDC 0363-7998 Antifungal Liquid Maximum Strength
Product NDC 0363-7998
11-digit product format 003637998
Labeler code 0363
Product ID 0363-7998_3bcf11d1-5417-a865-e063-6294a90ab771
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form LIQUID
Route TOPICAL
Labeler Walgreens Company
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-03-12
Marketing end 2026-11-30
Substance TOLNAFTATE
Active strength 10 mg/mL
NDC exclude flag No
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 Antifungal Liquid Maximum Strength 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 0363-7998-01 Antifungal Liquid Maximum Strength 1 in 1 CARTON LIQUID 1 5 0363-7998-01 Antifungal Liquid Maximum Strength 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 0363-7998 ANTIFUNGAL LIQUID MAXIMUM STRENGTH (TOLNAFTATE) LIQUID [WALGREENS COMPANY] 4 Current NDC, 2 package rows 20241215_137eabb7-cb4f-1631-e063-6294a90ab847.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 47 of 49 · 969 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0363-7998-01 00363799801 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0363-7998-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR 2024-03-12 2026-11-30 No No Historical