Home NDC 72937-004 MENTHOL
Product NDC 72937-004
11-digit product format 729370004
Labeler code 72937
Product ID 72937-004_44141d2a-1d91-b970-e063-6294a90a53f4
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler SUNSET PAIN RELIEF ROLL-ON 3OZ
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-09-24
Marketing end 2026-10-23
Substance MENTHOL, UNSPECIFIED FORM
Active strength 4 g/100mL
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 MENTHOL Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 4 g/100mL
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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72937-004-03 MENTHOL 90 mL in 1 BOTTLE, WITH APPLICATOR GEL 90 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72937-004 MENTHOL GEL [SUNSET PAIN RELIEF ROLL-ON 3OZ] 3 Current NDC, 1 package rows 20240129_934d4638-b47b-187d-e053-2995a90ae69d.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 73 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 72937-004-03 72937000403 90 mL in 1 BOTTLE, WITH APPLICATOR 90 ml Historical