Home NDC 72764-004-01 Pain Relieving Foot
Product NDC 72764-004
Requested package NDC 72764-004-01
11-digit product format 727640004
Labeler code 72764
Product ID 72764-004_f6ebe75b-a4c9-48f4-ae63-2677a83dcc96
Type HUMAN OTC DRUG
Nonproprietary name MENTHYL SALICYLATE and MENTHOL, UNSPECIFIED FORM
Dosage form CREAM
Route TOPICAL
Labeler Brandable
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-04-01
Marketing end 0000-00-00
Substance MENTHYL SALICYLATE, (+/-)-; MENTHOL, UNSPECIFIED FORM
Active strength 750 mg/5g; mg/5g
NDC exclude flag No
Listing certified through 2021-12-31
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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72764-004-01 Pain Relieving Foot 85 g in 1 CONTAINER CREAM 85 1 72764-004-01 Pain Relieving Foot 1 in 1 BOX CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72764-004 PAIN RELIEVING FOOT (MENTHYL SALICYLATE AND MENTHOL, UNSPECIFIED FORM) CREAM [BRANDABLE] 1 Legacy NDC, 2 package rows 20200401_952efa89-9115-4754-8213-d403ec854464.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72764-004-01 72764000401 1 CONTAINER in 1 BOX (72764-004-01) > 85 g in 1 CONTAINER 1 container 2020-04-01 0000-00-00 No No Current