Equate Pain Relief Balm

Product NDC: 79903-105
11-digit product format: 799030105
Labeler code: 79903
Product ID: 79903-105_40aa5ef9-be48-5f8d-e063-6294a90a68a3
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol 11%, Camphor 11% Ointment
Dosage form: OINTMENT
Route: TOPICAL
Labeler: WALMART, INC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-04-01
Substance: MENTHOL; CAMPHOR (SYNTHETIC)
Active strength: 110; 110 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
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
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product	79903-105		I	Inactivated by FDA		excluded / ndc_excluded.zip	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	79903-105	79903-105-18	I	Inactivated by FDA		excluded / ndc_excluded.zip	`1332a3947898…`	`d4bfe170f9cd…`

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 Pain Relief Balm
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	110 mg/g
CAMPHOR (SYNTHETIC)	110 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1089847	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
d8ddf835-f008-ce1f-e053-2a95a90aa9b3	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2024-03-15	EQUATE ULTRA STRENGTH PAIN RELIEF BALM – MENTHOL 11% & CAMPHOR 11%
2024-03-15	EQUATE ULTRA STRENGTH PAIN RELIEF BALM – MENTHOL 11% & CAMPHOR 11%
2024-01-30	EQUATE ULTRA STRENGTH PAIN RELIEF BALM – MENTHOL 11% & CAMPHOR 11%
2024-01-30	EQUATE ULTRA STRENGTH PAIN RELIEF BALM – MENTHOL 11% & CAMPHOR 11%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79903-105-18	Equate Pain Relief Balm	1 in 1 CARTON	OINTMENT	1		5
79903-105-18	Equate Pain Relief Balm	18 g in 1 BOTTLE, GLASS	OINTMENT	18		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79903-105	EQUATE PAIN RELIEF BALM (MENTHOL 11%, CAMPHOR 11% OINTMENT) OINTMENT [WALMART, INC]	4	Current NDC, Legacy NDC, 2 package rows	20240317_d8ddf835-f008-ce1f-e053-2a95a90aa9b3.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 136 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SUPER WHITE STUFF Pain Relief	MENTHOL	BLUE SPRING WELLNESS	e6d27df5-118c-4c6d-86e8-7b4401a39c76	2024-01-23	Warnings	Exact identifier application number: M017
Burn First Aid	BURN FIRST AID	Dynarex Corporation	826e08be-dffa-5a27-e053-2a91aa0a8701	2024-01-22	Warnings	Exact identifier application number: M017
Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On	MENTHOL	TARGET CORPORATION	0f95fc55-8665-9e89-e063-6394a90a7891	2024-01-22	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain Relief Plus Menthol	LIDOCAINE, MENTHOL, UNSPECIFIED FORM	Natural Essentials, Inc.	77978069-a1b4-473e-83c9-8320e00eea89	2024-01-19	Warnings	Exact identifier application number: M017
ZIMS MAX FREEZE LEG CRAMPS	CAMPHOR, MENTHOL	KOBAYASHI Healthcare International, Inc.	ba26635d-95d3-4d88-93cc-1fd4fd29fd79	2024-01-18	Warnings	Exact identifier application number: M017
Burn	LIDOCAINE	HART Health	e95ebdac-9789-41c2-97da-2307e4538794	2024-01-18	Warnings	Exact identifier application number: M017
Medi-First Hydrocortisone 1%	HYDROCORTISONE ACETATE	Unifirst First Aid Corporation	bd216f5d-f304-7d8d-e053-2a95a90aa9ce	2024-01-17	Warnings	Exact identifier application number: M017
Green Guard Hydrocortisone 1%	HYDROCORTISONE	Unifirst First Aid Corporation	bd348e2a-57b1-3f17-e053-2a95a90a8bdc	2024-01-17	Warnings	Exact identifier application number: M017
Pain Relief	LIDOCAINE, MENTHOL	HUMN Pharmaceuticals Inc	6c96f94a-e724-eab3-e053-2991aa0aab88	2024-01-17	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain Relief	LIDOCAINE	Natural Essentials, Inc.	52e82e70-53b7-4ecb-be39-fe10c94cc444	2024-01-17	Warnings	Exact identifier application number: M017
CVS Health XL Lidocaine Pain Relief	LIDOCAINE	NATURAL ESSENTIALS, INC.	ec16da91-8244-402b-b8d8-84896094ac2c	2024-01-17	Warnings	Exact identifier application number: M017
Anti-itch	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Target Corporation	f444b0a6-2ed3-4236-8206-342150290675	2024-01-17	Warnings	Exact identifier application number: M017
Maximum Strength Hydrocortisone Anti-itch	HYDROCORTISONE 1%	Target Corporation	4ff39cb8-3a20-4fe7-9829-1e882a484668	2024-01-17	Warnings	Exact identifier application number: M017
Burn	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	eca272cb-ac8f-982b-e053-2995a90aa8b2	2024-01-15	Warnings	Exact identifier application number: M017
American Safety and First Aid	HYDROCORTISONE ACETATE	Orazen Inc	eb0cfde0-c463-e9b5-e053-2a95a90a1924	2024-01-15	Warnings	Exact identifier application number: M017
American Safety and First Aid	HYDROCORTISONE ACETATE	Orazen Inc	eb0cce4b-c70a-1b2d-e053-2995a90aa4aa	2024-01-15	Warnings	Exact identifier application number: M017
Oral Pain Relief Gel	BENZOCAINE 20%	Sled Distribution, LLC	e7391302-831e-14dc-e053-2a95a90ac236	2024-01-15	Warnings	Exact identifier application number: M017
FIRST SHIELD	LIDOCAINE HCI	Ever Ready First Aid	e022bf8f-3dd8-de22-e053-2995a90a219b	2024-01-15	Warnings	Exact identifier application number: M017
Flexigen	MENTHOL 1.25%	Derma Care Research Labs, LLC	e9ae2682-59b4-e796-e053-2995a90af921	2024-01-15	Warnings	Exact identifier application number: M017
Vita-P Oral and Nasal	MENTHOL 1%	Beijing HKKY Medical Tech. Co., Ltd.	537c3843-1c92-41c6-b724-52701bbddeab	2024-01-13	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1089847	camphor 11 % / menthol 11 % Topical Ointment	PSN	d8ddf835-f008-ce1f-e053-2a95a90aa9b3	5
1089847	camphor 0.11 MG/MG / menthol 0.11 MG/MG Topical Ointment	SCD	d8ddf835-f008-ce1f-e053-2a95a90aa9b3	5
1089847	camphor 11 % / menthol 11 % Topical Ointment	SY	d8ddf835-f008-ce1f-e053-2a95a90aa9b3	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
79903-105-18	79903010518	1 BOTTLE, GLASS in 1 CARTON (79903-105-18) / 18 g in 1 BOTTLE, GLASS	2022-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
EQUATE ULTRA STRENGTH PAIN RELIEF BALM – MENTHOL 11% & CAMPHOR 11%	WALMART, INC	2025-10-08	HUMAN OTC DRUG LABEL	5