Home NDC 72937-013 MENTHOL, CAMPHOR
Product NDC 72937-013
11-digit product format 729370013
Labeler code 72937
Product ID 72937-013_5980c527-6bcc-a846-e063-6294a90a0788
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, CAMPHOR
Dosage form CREAM
Route TOPICAL
Labeler SUNSET PAIN RELIEF
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-20
Substance MENTHOL, UNSPECIFIED FORM; CAMPHOR (NATURAL)
Active strength 10; 3 g/100g; 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 MENTHOL, CAMPHOR
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 10 g/100g CAMPHOR (NATURAL) 3 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup N20HL7Q941 Internal UNII 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 72937-013-08 72937001308 237 g in 1 JAR (72937-013-08) 237 g 2026-08-20 No No Current