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#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-01-27	Top Care Menthol Foot Powder Talc Free
2023-01-27	Top Care Menthol Foot Powder Talc Free
2023-01-27	Top Care Menthol Foot Powder Talc Free
2022-07-29	Top Care Menthol Foot Powder Talc Free
2022-07-29	Top Care Menthol Foot Powder Talc Free
2022-07-29	Top Care Menthol Foot Powder Talc Free

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 23 of 156 · 3,115 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eagle Brand Medicated Roll On Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	PT. EAGLE INDO PHARMA	0f333f93-bec6-72d5-e063-6394a90a4e3f	2026-04-27	Warnings	Exact identifier application number: M017
HIP PAIN RELIEF ROLL-ON	LIDOCAINE AND MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	502f1f9e-8552-ca7b-e063-6394a90a7c53	2026-04-24	Warnings	Exact identifier application number: M017
SOMBRA WARM THERAPY	MENTHOL CAMPHOR	SOMBRA COSMETICS INC.	de78dba9-53b3-4dbd-9dd2-6a692378da34	2026-04-24	Warnings	Exact identifier application number: M017
Rite Aid Itch Relief	DIPHENHYDRAMINE HCL 2%, ZINC ACETATE 0.1%	Rite Aid	e285df43-317c-d862-e053-2a95a90acdce	2026-04-23	Warnings	Exact identifier application number: M017
FixMySkin Healing Balm Unflavored	HYDROCORTISONE	Lovely Skin, Inc.	9ff8db07-ad6d-4865-a534-94bd8312957e	2026-04-23	Warnings	Exact identifier application number: M017
DCH Labs Cortisone	HYDROCORTISONE 1%	Derma Care Research Labs	5025f53a-02e0-0f6a-e063-6394a90adbbf	2026-04-23	Warnings	Exact identifier application number: M017
Hydrocortisone 1%	HYDROCORTISONE	Preferred Pharmaceuticals Inc.	e0f46445-64c5-4f5d-90b0-3fa07ed7d1b4	2026-04-22	Warnings	Exact identifier application number: M017
Dr. Carrasco Pain Relief	MENTHOL	Carrasco Enterprises, Inc.	befa8526-f468-428e-a829-422c2ea48612	2026-04-21	Warnings	Exact identifier application number: M017
HealthWise Feminine Anti-itch Cream	BENZOCAINE, RESORCINOL	Veridian Healthcare	4ff88b9e-5869-a1cb-e063-6294a90a87b7	2026-04-21	Warnings	Exact identifier application number: M017
SOMBRA COOL THERAPY	MENTHOL	SOMBRA COSMETICS INC.	87e9b16b-1cab-48f7-b9e4-1c3eaeeb3ca3	2026-04-21	Warnings	Exact identifier application number: M017
Careland Lidocaine Pain Relieving	LIDOCAINE	Planet (Anhui) Pharmaceutical Co., Ltd.	c4c86a8f-1d57-49d2-a65f-acb0dccf2f87	2026-04-21	Warnings	Exact identifier application number: M017
KOXUO Arnica Bruise Cream	ARNICA BRUISE CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	5003bf83-fa01-b01a-e063-6294a90ad37f	2026-04-21	Warnings	Exact identifier application number: M017
KT Pain Relief Cream Magnesium with Arnica and 4% Lidocaine	KT PAIN RELIEF CREAM MAGNESIUM WITH ARNICA AND 4% LIDOCAINE ROLLON	Clarion Brands LLC	4f82993c-ebc4-5787-e063-6294a90a12d6	2026-04-20	Warnings	Exact identifier application number: M017
KT Pain Relief Cream Magnesium with Cooling 5% Menthol	KT PAIN RELIEF CREAM MAGNESIUM WITH COOLING 5% MENTHOL	Clarion Brands LLC	4fe64056-f3c6-bc76-e063-6294a90a7e62	2026-04-20	Warnings	Exact identifier application number: M017
Kevo-Prophen	JUNIPER TAR	Faeve, LLC	4fe773a8-77cd-831e-e063-6294a90ae2ca	2026-04-20	Warnings	Exact identifier application number: M017
BeeVenom	METHYL SALICYLATE	Menper Distributors, Inc.	4fe7a986-336d-ad4e-e063-6294a90a0b8a	2026-04-20	Warnings	Exact identifier application number: M017
Benzodent	BENZOCAINE	Focus Consumer Healthcare, LLC	5fdcb871-d387-6352-e053-2991aa0a09da	2026-04-20	Warnings	Exact identifier application number: M017
Tecnu Calagel	DIPHENHYDRAMINE HYDROCHLORIDE	Tec Laboratories Inc.	8bc9cbfe-1dd4-18ed-e053-2a95a90a7966	2026-04-20	Warnings	Exact identifier application number: M017
Aemerry Numbing Cream	MENTHOL 5%	Da Capo Prima LLC	4fefddaf-19c8-86b4-e063-6294a90abffc	2026-04-20	Warnings	Exact identifier application number: M017
Sting Relief Swab	BENZOCAINE	4 Visions LLC	4fc7a356-2f1d-85af-e063-6394a90aec6b	2026-04-18	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	7caef8db-a07a-6705-e053-2991aa0aa724	7
259579	menthol 0.01 MG/MG Topical Powder	SCD	7caef8db-a07a-6705-e053-2991aa0aa724	7
259579	menthol 1 % Topical Powder	SY	7caef8db-a07a-6705-e053-2991aa0aa724	7

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