Home NDC 36800-252 Menthol
Product NDC 36800-252
11-digit product format 368000252
Labeler code 36800
Product ID 36800-252_5ccea69a-bfc7-4068-e063-6394a90a177b
Type HUMAN OTC DRUG
Nonproprietary name Maximum Strength Medicated Foot Powder Talc Free
Dosage form POWDER
Route TOPICAL
Labeler Topco Associates LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-02-10
Substance MENTHOL
Active strength 2.8 g/283g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 2 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 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product 36800-252 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 36800-252 36800-252-10 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…
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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 2.8 g/283g
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 36800-252-10 Menthol 283 g in 1 BOTTLE, PLASTIC POWDER 283 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 36800-252 MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [TOPCO ASSOCIATES LLC] 6 Current NDC, Legacy NDC, 1 package rows 20241213_7caef8db-a07a-6705-e053-2991aa0aa724.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 86 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Freds Hydrocortisone Plus 12 Moisturizers HYDROCORTISONE FRED'S, INC. 7502eebe-11c5-4e9e-b427-b87180a84349 2025-07-16 Warnings Exact identifier application number: M017 PROINNATE Numbing Cream MENTHOL Guangzhou Haishi Biological Technology Co., Ltd. 39688b2b-c1fe-cd86-e063-6394a90a5345 2025-07-16 Warnings Exact identifier application number: M017 Methyl Salicylate METHYL SALICYLATE ViolaCare, Inc. 8f0ba6e7-8aa4-443e-99ae-a255085ddfec 2025-07-15 Warnings Exact identifier application number: M017 TopCare Hydrocortisone Intensive Healing Formula HYDROCORTISONE Topco Associates LLC 7daafc44-e2a4-4f1b-bfca-3309a8e9a920 2025-07-15 Warnings Exact identifier application number: M017 Hydrocortisone Plus 12 Moisturizers HYDROCORTISONE TARGET Corporation 72c3889c-b743-4728-a315-6e4063e00200 2025-07-15 Warnings Exact identifier application number: M017 Shopko Hydrocortisone Maximum Strength HYDROCORTISONE Shopko Stores Operating Co., LLC 0431a6af-4c9a-4bbd-a535-cba31a5e53cc 2025-07-15 Warnings Exact identifier application number: M017 Freds Hydrocortisone with Aloe HYDROCORTISONE FRED'S, INC. 076503bf-8238-4739-bb1c-c385e72f8a96 2025-07-15 Warnings Exact identifier application number: M017 Shopko Hydrocortisone HYDROCORTISONE Shopko Stores Operating Co., LLC 92bcbde3-401a-4301-854e-c352852317d6 2025-07-15 Warnings Exact identifier application number: M017 TopCare Hydrocortisone HYDROCORTISONE Topco Associates LLC bd3585fa-3b48-49b7-8ad1-749bf1e31ed5 2025-07-15 Warnings Exact identifier application number: M017 Methyl Salicylate 25% Pain Relieving METHYL SALICYLATE Puretek Corporation 376797ff-cf13-a3c6-e063-6394a90a9de1 2025-07-15 Warnings Exact identifier application number: M017 TIGER BALM PAIN RELIEVING CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM Haw Par Healthcare Ltd. 440e97bc-bd97-4733-9955-643b18e7fb18 2025-07-15 Warnings Exact identifier application number: M017 Tiger Balm Pain Relieving Hydrogel Large CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM Haw Par Healthcare Ltd. 064d04ca-184d-492b-867c-beaa165ab3e0 2025-07-14 Warnings Exact identifier application number: M017 Methyl Salicylate 25% Cream METHYL SALICYLATE Medcore LLC 143f76bf-2de4-466a-8a6b-d6ab6314a2c3 2025-07-14 Warnings Exact identifier application number: M017 BLUESPRING Doctors Pain Formula Pain Relief MENTHOL ACA MANAGEMENT LLC 98f3f719-792f-4a93-95b1-90072e0f8bf4 2025-07-14 Warnings Exact identifier application number: M017 Shopko Anti-Itch DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE Shopko Stores Operating Co., LLC 130119eb-b87e-4a07-8d2a-317369bfa541 2025-07-14 Warnings Exact identifier application number: M017 Equate Hydrocortisone Intensive Healing Formula HYDROCORTISONE Wal-Mart Stores Inc. 635b49c4-54d2-4b6d-bee8-851fc2c7ca9c 2025-07-14 Warnings Exact identifier application number: M017 ULTRA STRENGTH ZHENG GU SHUI MENTHOL AND CAMPHOR GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD 53397663-044d-4e48-989b-2c6257af5f84 2025-07-14 Warnings, Adverse reactions Exact identifier application number: M017 TIGER BALM PAIN RELIEVING HYDROGEL CAMPHOR (SYNTHETIC), LEVOMENTHOL, AND CAPSICUM Haw Par Healthcare Ltd. cb60037f-bceb-4090-a5e4-bdda0cbf9f5c 2025-07-14 Warnings Exact identifier application number: M017 Avedana Hydrocortisone Cream with Aloe HYDROCORTISONE Unipack LLC 2a55c426-39b4-4d94-b6b4-6c548c9685e9 2025-07-13 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE ACETATE Rite Aid Corporation cb6e0bed-2ea1-49d2-89e7-2554e7565b74 2025-07-11 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 36800-252-10 36800025210 283 g in 1 BOTTLE, PLASTIC (36800-252-10) 283 g 2019-02-10 0000-00-00 No No Current