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 21 of 156 · 3,115 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join BonicaEaseX Pain Relieving Lidocaine LIDOCAINE Planet (Anhui) Pharmaceutical Co., Ltd. 7486fe89-a377-4a37-997d-e3bd16b891a7 2026-05-11 Warnings Exact identifier application number: M017 YYSDMVY NUMBING Cream LIDOCAINE 4% NUMBING CREAM Jiangxi Yudexi Pharmaceutical Co., LTD 5195f5ec-8524-77f5-e063-6294a90abdc2 2026-05-11 Warnings Exact identifier application number: M017 Lightning X Burn Relief Gel LIDOCAINE HYDROCHLORIDE Nantong Health & Beyond Hygienic Products Inc. 515eb4cc-63af-c11d-e063-6294a90a13ca 2026-05-09 Warnings Exact identifier application number: M017 Albertson Lidocaine, Menthol Pain Relief Medicated Patch LIDOCAINE AND MENTHOL Safeway dc647647-90ec-6beb-e053-2a95a90a7982 2026-05-09 Warnings Exact identifier application number: M017 5 Elementum Lidocaine Male Genital Desensitizer LIDOCAINE MALE GENITAL DESENSITIZER MSVENTURESGROUP O 514b1738-886e-a95d-e063-6294a90aa707 2026-05-08 Warnings Exact identifier application number: M017 Kroger Muscle Rub Cream MENTHOL, CAMPHOR, METHYL SALICYLATE Kroger Co. 45c8c79a-b4b4-d4be-e063-6394a90a9251 2026-05-08 Warnings Exact identifier application number: M017 Walmart Equate Aloe Sunburn Relief Cooling LIDOCAINE WAL-MART STORES INC. 51540f6b-596f-bc47-e063-6294a90a46ae 2026-05-08 Warnings Exact identifier application number: M017 Capsaicin 0.035% cream CAPSAICIN Medcore LLC 0236e1e4-c26c-4fff-a83b-143ce26d93bf 2026-05-07 Warnings Exact identifier application number: M017 Lidocaine 4% Cream LIDOCAINE Medcore LLC 111cb421-ba3b-4772-ab60-d31eb4183168 2026-05-07 Warnings Exact identifier application number: M017 Lidocaine 5% Cream LIDOCAINE Medcore LLC 15d02b42-bf8b-486a-a081-f6d17cc11ec7 2026-05-07 Warnings Exact identifier application number: M017 JenGufun LIDOCAINE Pain Relief Gel-Patch LIDOCAINE PAIN RELIEF GEL-PATCH Henan Kangdi Medical Devices Co., Ltd. 51363a41-5dcc-6a3b-e063-6294a90a6c27 2026-05-07 Warnings Exact identifier application number: M017 Lidoxi LIDOCAINE T&T Pharma Holdings LLC 513c517e-c098-02aa-e063-6294a90ac8a4 2026-05-07 Warnings Exact identifier application number: M017 Harris Teeter Hydrocortisone HYDROCORTISONE HARRIS TEETER LLC 4e8199f8-96ec-5342-e063-6294a90afb2d 2026-05-07 Warnings Exact identifier application number: M017 CAREALL Hydrocortisone Maximum Strength HYDROCORTISONE New World Imports, Inc. 5114cdba-96a1-c399-e063-6294a90aac12 2026-05-06 Warnings Exact identifier application number: M017 New Terocin METHYL SALICYLATE, CAPSAICIN, AND MENTHOL ASCLEMED USA INC. 68dc0231-3364-448b-bde9-f19fa122c765 2026-05-05 Warnings Exact identifier application number: M017 Lidocaine 4% Patch LIDOCAINE 4% SOLA Pharmaceuticals c31957dd-edea-ce98-e053-2a95a90a9c2d 2026-05-05 Warnings Exact identifier application number: M017 Biofreeze Triple Target Gel CAMPHOR, CAPSAICIN, MENTHOL Reckitt Benckiser LLC 511852c8-7428-3234-e063-6394a90a5bc2 2026-05-05 Warnings Exact identifier application number: M017 5Kind DMSO Pain Relieving CAMPHOR (SYNTHETIC) 5Kind Trading LTD 62b55114-47f4-473a-8406-78238c3c1fa2 2026-05-04 Warnings Exact identifier application number: M017 Zinc Oxide with Menthol and White Petrolatum MENTHOL, ZINC OXIDE, WHITE PETROLATUM Aldermed Inc. f993fc0a-bd80-4345-a948-65ac03f910e2 2026-05-04 Warnings Exact identifier application number: M017 EVERLIT CARE PRODUCTS BURN RELIEF LIDOCAINE HYDROCHLORIDE EVERLIT GLOBAL INC. d7ec5720-4d1f-4943-ae36-c7d6acbae7d7 2026-05-04 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