Home NDC 72246-112-01 Dr. Ds Super 7 Pain Relief
Product NDC 72246-112
Requested package NDC 72246-112-01
11-digit product format 722460112
Labeler code 72246
Product ID 72246-112_b9e9ab5b-aff7-e8cf-e053-2995a90a93f5
Type HUMAN OTC DRUG
Nonproprietary name menthyl salicylate and menthol
Dosage form CREAM
Route TOPICAL
Labeler Promedx Innovations Inc
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2019-09-04
Marketing end 0000-00-00
Substance MENTHOL; MENTHYL SALICYLATE, (+/-)-
Active strength 20 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2022-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72246-112 DR. DS SUPER 7 PAIN RELIEF (MENTHYL SALICYLATE AND MENTHOL) CREAM [PROMEDX INNOVATIONS INC] 2 Legacy NDC 20210129_aaca1fbf-aed6-4fe0-9821-6fa897b5d41e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 72246-112-01 72246011201 1 BOTTLE, WITH APPLICATOR in 1 CARTON (72246-112-01) > 88 mL in 1 BOTTLE, WITH APPLICATOR 2019-09-04 0000-00-00 No No Current