Home NDC 72937-010 MENTHOL, CAMPHOR
Product NDC 72937-010
11-digit product format 729370010
Labeler code 72937
Product ID 72937-010_43fee6fe-06a0-4d07-e063-6294a90a9529
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 2019-05-24
Marketing end 2027-06-25
Substance MENTHOL, UNSPECIFIED FORM; CAMPHOR (NATURAL)
Active strength 10; 3 g/100g; g/100g
NDC exclude flag No
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 72937-010 72937-010-16 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 72937-010 72937-010-04 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 72937-010 72937-010-02 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72937-010-02 MENTHOL, CAMPHOR 57 g in 1 JAR CREAM 57 22 72937-010-04 MENTHOL, CAMPHOR 113 g in 1 JAR CREAM 113 22 72937-010-08 MENTHOL, CAMPHOR 227 g in 1 JAR CREAM 227 22 72937-010-16 MENTHOL, CAMPHOR 454 g in 1 JAR CREAM 454 22
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72937-010 MENTHOL, CAMPHOR CREAM [SUNSET PAIN RELIEF] 21 Current NDC, 4 package rows 20241122_89f5f688-856f-f2df-e053-2995a90a73cf.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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72937-010-02 72937001002 57 g in 1 JAR 57 g Historical 72937-010-04 72937001004 113 g in 1 JAR 113 g Historical 72937-010-08 72937001008 227 g in 1 JAR (72937-010-08) 227 g 2023-09-15 2027-06-19 No No Historical 72937-010-16 72937001016 454 g in 1 JAR 454 g Historical