Menthol

Product NDC: 81522-069
Requested package NDC: 81522-069-01
11-digit product format: 815220069
Labeler code: 81522
Product ID: 81522-069_422aaf23-440e-34a8-e063-6294a90a215d
Type: HUMAN OTC DRUG
Nonproprietary name: Maximum Strength Medicated Foot Powder Talc Free
Dosage form: POWDER
Route: TOPICAL
Labeler: FSA Store Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-05-02
Substance: MENTHOL
Active strength: 10 mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	10 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
259579	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
fb3548c8-f202-dc50-e053-6394a90a5b30	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81522-069-01	Menthol	283 g in 1 BOTTLE, PLASTIC	POWDER	283		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81522-069	MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [FSA STORE INC.]	3	Current NDC, 1 package rows	20241109_fb3548c8-f202-dc50-e053-6394a90a5b30.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 79 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
KNEE PAIN RELIRF Patch	CAMPHOR, MENTHOL	Shenzhen Finona Information Technology Co., Ltd	3db971ef-d7fa-0171-e063-6294a90aa58b	2025-09-01	Warnings	Exact identifier application number: M017
Bikini Zone Medicated Creme	LIDOCAINE	Kingsway Pharmaceuticals dba NFI, LLC	300ac57e-844a-4840-b285-41ff5518e6b6	2025-08-29	Warnings	Exact identifier application number: M017
Bikini Zone Medicated Gel	LIDOCAINE	Kingsway Pharmaceuticals dba NFI, LLC	30b85890-e72d-4af7-bda9-e7744abc92af	2025-08-29	Warnings	Exact identifier application number: M017
Sumifun Lidocaine Pain Relief Gel-Patch	LIDOCAINE	Guangzhou Zhupuyou E-commerce Co., Ltd	3d7dc8cc-0680-d94d-e063-6394a90ac8e8	2025-08-29	Warnings	Exact identifier application number: M017
TKTALKER NUMBING	NUMBING	Shenzhen Shandian Jingling Technology Co., Ltd.	3d7e6757-f183-2a68-e063-6294a90ae4ca	2025-08-29	Warnings	Exact identifier application number: M017
PBZ OTC	TRIPELENNAMINE HCL 1%	Kingsway Pharmaceuticals dba NFI, LLC	12f72d74-018f-4bc6-acd4-175ca3af4c6d	2025-08-29	Warnings	Exact identifier application number: M017
else.	LIDOCAINE	Else Co.	3d6c7b10-ed03-bbde-e063-6294a90ae92f	2025-08-28	Warnings	Exact identifier application number: M017
Mountain Ice Pain Relief	MENTHOL	Mountainside Medical Equipment, Inc.	c79fdd91-16f4-4ae0-bee4-d37c05ed2074	2025-08-28	Warnings	Exact identifier application number: M017
HealthWise 4% Lidocaine Cream 2.7 oz	LIDOCAINE HYDROCHLORIDE	Veridian Healthcare	f39eb3d0-e153-4f50-85b1-ad5c677d176c	2025-08-28	Warnings	Exact identifier application number: M017
HealthWise Overnight Menthol Patch	MENTHOL	Veridian Healthcare	6379f50d-2878-46ca-8acb-71c4554585e9	2025-08-28	Warnings	Exact identifier application number: M017
Anti Itch Maximum Relief	PRAMOXINE HYDROCHLORIDE AND MENTHOL	Natureplex LLC	75de3d5e-ecbe-4d04-a39d-792200e6ee32	2025-08-28	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	3d5718f3-c175-6b64-e063-6394a90aa6f1	2025-08-27	Warnings	Exact identifier application number: M017
ARCTIC HEAT	MENTHOL, METHYL SALICYLATE	Renu Laboratories, LLC	402df5c1-b8cb-17a2-e054-00144ff8d46c	2025-08-27	Warnings	Exact identifier application number: M017
PROHEAL HYDROCORTISONE 1% MAXIMUM STRENGTH PLUS ALOE	HYDROCORTISONE	Click Industries LLC	328c389c-7e05-4892-a9b3-b6a753f4935a	2025-08-25	Warnings	Exact identifier application number: M017
Yeheal	CAMPHOR, MENTHOL, ISOPROPYL ALCOHOL	Shenzhen Yeheal Biotechnology Co., Ltd	3cf1bc74-3060-6d63-e063-6294a90a9f5c	2025-08-22	Warnings	Exact identifier application number: M017
Dermedial Anti-Ouch	MENTHOL	Natures Formulae Health Products Ltd.	3ce29160-3964-e435-e063-6394a90abb38	2025-08-21	Warnings	Exact identifier application number: M017
SUGARLOAF ORGANICS MENTHOL REVIVE	MENTHOL	RENU LABORATORIES, LLC	fa2f9539-b703-a00b-e053-6394a90ae309	2025-08-21	Warnings	Exact identifier application number: M017
Camphor 4% Plus Menthol 10%	CAMPHOR 4% PLUS MENTHOL 10%	PureTek Corporation	3cab26e4-e377-f26a-e063-6394a90a17af	2025-08-20	Warnings	Exact identifier application number: M017
Capsaicin 0.035% Cream	CAPSAICIN 0.035% CREAM	Puretekcorp	3cbc73b6-8c58-8f23-e063-6394a90a71a3	2025-08-20	Warnings	Exact identifier application number: M017
Game On	MENTHOL, METHYL SALICYLATE	Natural Essentials, Inc.	3cd20f1f-033f-f698-e063-6294a90a89eb	2025-08-20	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
259579	menthol 1 % Topical Powder	PSN	fb3548c8-f202-dc50-e053-6394a90a5b30	4
259579	menthol 0.01 MG/MG Topical Powder	SCD	fb3548c8-f202-dc50-e053-6394a90a5b30	4
259579	menthol 1 % Topical Powder	SY	fb3548c8-f202-dc50-e053-6394a90a5b30	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
81522-069-01	81522006901	283 g in 1 BOTTLE, PLASTIC (81522-069-01)	283 g	2023-05-02	No	No	Current