Home NDC 72937-040-03 KANGAROO CBD PAIN RELIEVING
Product NDC 72937-040
Requested package NDC 72937-040-03
11-digit product format 729370040
Labeler code 72937
Product ID 72937-040_ef15ad44-6dc4-0c85-e053-2a95a90a6f10
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler SUNSET NOVELTIES, INC
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2022-12-05
Marketing end 0000-00-00
Substance MENTHOL
Active strength 4 g/100g
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 1 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 72937-040 72937-040-03 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72937-040 KANGAROO CBD PAIN RELIEVING (MENTHOL) GEL [SUNSET NOVELTIES, INC] 2 Legacy NDC 20241122_ef15acdb-1733-2b6d-e053-2a95a90ad3d4.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72937-040-03 72937004003 85 g in 1 TUBE (72937-040-03) 85 g 2022-12-05 0000-00-00 No No Current