Home NDC 72937-017 HEATING PAIN RELIEF
Product NDC 72937-017
11-digit product format 729370017
Labeler code 72937
Product ID 72937-017_498ce6da-8469-6b2a-e063-6294a90a9425
Type HUMAN OTC DRUG
Nonproprietary name METHYL SALICYLATE, MENTHOL
Dosage form CREAM
Route TOPICAL
Labeler SUNSET NOVELTIES, INC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-29
Substance MENTHOL; METHYL SALICYLATE
Active strength 10; 18 g/100mL; g/100mL
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 HEATING PAIN RELIEF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10 g/100mL METHYL SALICYLATE 18 g/100mL
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 LAV5U5022Y 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 72937-017-20 HEATING PAIN RELIEF 59 mL in 1 TUBE CREAM 59 2
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 Marketing start Sample Exclude flag Status 72937-017-20 72937001720 59 mL in 1 TUBE (72937-017-20) 59 ml 2026-01-29 No No Current