Home NDC 51316-519 Medicated BODY
Product NDC 51316-519
11-digit product format 513160519
Labeler code 51316
Product ID 51316-519_90fb0a8d-acc7-4b71-bdb3-4a3c8b644320
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form POWDER
Route TOPICAL
Labeler CVS Pharmacy, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-11
Substance MENTHOL
Active strength .15 g/100g
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 Medicated BODY
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL .15 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1431703 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51316-519-10 51316051910 283 g in 1 BOTTLE (51316-519-10) 283 g 2026-08-11 No No Current