Home NDC 51316-898 Maximum Strength Antifungal Liquid
Product NDC 51316-898
11-digit product format 513160898
Labeler code 51316
Product ID 51316-898_5c3feb72-9a02-1f4b-e063-6294a90a9295
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate
Dosage form LIQUID
Route TOPICAL
Labeler CVS Pharmacy
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-21
Substance TOLNAFTATE
Active strength .3 g/30mL
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 .3 g/30mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51316-898-00 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 51316-898 MAXIMUM STRENGTH ANTIFUNGAL LIQUID (TOLNAFTATE) LIQUID [CVS PHARMACY] 3 Current NDC, Legacy NDC, 1 package rows 20241115_e9315999-ca7a-18ea-e053-2a95a90a5b41.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 Units Marketing start Marketing end Sample Exclude flag Status 51316-898-00 51316089800 30 mL in 1 BOTTLE, WITH APPLICATOR (51316-898-00) 30 ml 2022-09-21 0000-00-00 No No Current