Equate Menthol Pain Relieving

Product NDC: 49035-870
11-digit product format: 490350870
Labeler code: 49035
Product ID: 49035-870_5a98d4a1-d1fa-355a-e063-6294a90a2f5b
Type: HUMAN OTC DRUG
Nonproprietary name: menthol
Dosage form: PATCH
Route: TOPICAL
Labeler: Wal-Mart Stores Inc
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-01-01
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 50 mg/1
NDC exclude flag: No
Listing certified through: 2027-12-31
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: Equate Menthol Pain Relieving
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	50 mg/1

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
420222	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
d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-04-14	Drug Facts -Equate Menthol Pain Relieving
2023-04-14	Drug Facts -Equate Menthol Pain Relieving
2023-01-30	Drug Facts -Equate Menthol Pain Relieving
2023-01-30	Drug Facts -Equate Menthol Pain Relieving

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49035-870-01	Equate Menthol Pain Relieving	1 in 1 POUCH	PATCH	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-870	EQUATE MENTHOL PAIN RELIEVING (MENTHOL) PATCH [WAL-MART STORES INC]	5	Current NDC, Legacy NDC, 1 package rows	20241219_d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc.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 67 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stallion	DELAY CREME	Novelties by Nasswalk, Inc.	0261ec88-8fe4-d5f8-e063-6294a90ab3d4	2025-11-10	Warnings	Exact identifier application number: M017
ANAL-ESE	DESENSITIZER	Novelties by Nasswalk, Inc.	03b89eed-b433-a263-e063-6294a90a675b	2025-11-10	Warnings	Exact identifier application number: M017
Instant Erection	ULTIMATE ERECTION ENHANCER	Novelties by Nasswalk, Inc.	03a444f9-7052-0c38-e063-6294a90a4e56	2025-11-10	Warnings	Exact identifier application number: M017
STA-HARD	DESENSITIZING LUBRICANT	Novelties by Nasswalk, Inc.	02ef794b-8e70-5c26-e063-6294a90a28d1	2025-11-10	Warnings	Exact identifier application number: M017
ANAL-ESE	DESENSITIZER	Novelties by Nasswalk, Inc.	03a4a7ce-4cff-a608-e063-6294a90ad65d	2025-11-10	Warnings	Exact identifier application number: M017
FOOTSPA PEDI	ALCOHOL	CHEMCO CORPORATION	04de4392-74f6-7df8-e063-6294a90ae3b1	2025-11-08	Warnings	Exact identifier application number: M017
Johnson and Johnson All Purpose First Aid Kit	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	5cdb47c5-7951-4279-8a05-0a3199d3dd45	2025-11-06	Warnings	Exact identifier application number: M017
Johnson and Johnson First Aid Travel Ready 80 CT	ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	f388f105-48ba-4616-e053-2a95a90a0049	2025-11-06	Warnings	Exact identifier application number: M017
Johnson and Johnson First Aid All Purpose 160 CT	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	f3933330-2550-4a88-e053-2a95a90a3997	2025-11-06	Warnings	Exact identifier application number: M017
Foot and Leg Pain Relief	LIDOCAINE	Premier Brands of America Inc.	42f23e2f-11c6-da49-e063-6294a90ac720	2025-11-06	Warnings	Exact identifier application number: M017
HEALING TREE CALMING ANTI-ITCH	HYDROCORTISONE	Renu Laboratories, LLC	fc8bcde9-26e8-a35f-e053-6394a90a3300	2025-11-06	Warnings	Exact identifier application number: M017
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	Chain Drug Marketing Association Inc	1a3f8819-58cf-8923-e063-6394a90a37af	2025-11-06	Warnings	Exact identifier application number: M017
Extra Strength Itch Relief	DIPHENHYDRAMINE HCL AND ZINC ACETATE	Chain Drug Marketing Association Inc	1a2997bc-7741-e658-e063-6394a90af6fd	2025-11-06	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF CONTINUOUS SPRAY	Topco Associates LLC	8026c7dd-eb7b-ebea-e053-2991aa0a1b0f	2025-11-06	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF	Walgreen Company	6057b4ff-6adc-4688-893c-62d237d7d1ae	2025-11-06	Warnings	Exact identifier application number: M017
BANPINGHUA Glucosamine Chondroitin Patch	PEPPERMINT, CAMPHOR, BORNEOL	Henan Lijitang Medical Technology Co., Ltd.	42f8c2ae-50a2-2358-e063-6394a90a5979	2025-11-06	Warnings	Exact identifier application number: M017
PAINGEL	CAMPHOR, MENTHOL	NACOR BUSINESS GROUP LLC	42fa2397-b61a-3b16-e063-6294a90a5fed	2025-11-06	Warnings	Exact identifier application number: M017
PAINGEL UNGUENTO	CAMPHOR, MENTHOL	NACOR BUSINESS GROUP LLC	42fab525-b0a5-97fb-e063-6394a90aec6c	2025-11-06	Warnings	Exact identifier application number: M017
PAINGEL ROLL-ON	MENTHOL	NACOR BUSINESS GROUP LLC	42fb0bdf-8bbd-bbe3-e063-6294a90a656c	2025-11-06	Warnings	Exact identifier application number: M017
Coolexa	CAMPHOR, MENTHOL, METHYL SALICYLATE	Rising Pharma Holdings, Inc.	38839f29-d4ce-4684-a3c7-0bb4bf1ad594	2025-11-06	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
420222	menthol 5 % Medicated Patch	PSN	d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc	5
420222	menthol 0.05 MG/MG Medicated Patch	SCD	d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc	5
420222	menthol 5 % Medicated Patch	SY	d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49035-870-01	49035087001	1 PATCH in 1 POUCH (49035-870-01)	1 patch	2018-01-01	0000-00-00	No	No	Current