Medique Back Pain Relief

Product NDC: 47682-074
11-digit product format: 476820074
Labeler code: 47682
Product ID: 47682-074_3e4cc387-246f-c235-e063-6294a90aaa86
Type: HUMAN OTC DRUG
Nonproprietary name: Magnesium Salicylate Tetrahydrate
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Unifirst First Aid Corporation
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-09-26
Substance: MAGNESIUM SALICYLATE
Active strength: 580 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	47682-074		D	Discontinued by firm	2026-10-05
excluded package	package	47682-074	47682-074-33	D	Discontinued by firm	2026-10-05
excluded package	package	47682-074	47682-074-99	D	Discontinued by firm	2026-10-05

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 · 36 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	47682-074-33	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	47682-074-99	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	47682-074-33	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	47682-074-99	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	47682-074-33	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	47682-074-99	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	47682-074-33	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	47682-074-99	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	47682-074-33	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	47682-074-99	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	47682-074-33	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	47682-074-99	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	47682-074-33	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	47682-074-99	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	47682-074-33	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	47682-074-99	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	47682-074-33	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	47682-074-99	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	47682-074-33	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	47682-074-99	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	47682-074-33	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	47682-074-99	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	47682-074-33	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	47682-074-99	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Medique Back Pain Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MAGNESIUM SALICYLATE	580 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
41728CY7UX	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198742	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
e5563a0a-776a-83d4-e053-2a95a90a9500	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
47682-074-36	Medique Back Pain Relief	75 in 1 BOX	TABLET, FILM COATED	75	5
47682-074-36	Medique Back Pain Relief	2 in 1 PACKET	TABLET, FILM COATED	2	5
47682-074-80	Medique Back Pain Relief	40 in 1 BOX	TABLET, FILM COATED	40	5
47682-074-99	Medique Back Pain Relief	2 in 1 PACKET	TABLET, FILM COATED	2	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47682-074	MEDIQUE BACK PAIN RELIEF (MAGNESIUM SALICYLATE TETRAHYDRATE) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION]	4	Current NDC, Legacy NDC, 4 package rows	20240915_e5563a0a-776a-83d4-e053-2a95a90a9500.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 9 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aspirin Low Dose	ASPIRIN	ARMY AND AIR FORCE EXCHANGE SERVICE	e273ead7-7cbc-4fd5-a136-9d3558a35360	2026-06-24	Warnings	Exact identifier application number: M013
Acetaminophen Regular Strength	ACETAMINOPHEN	CVS PHARMACY	5e35df92-6282-4ca6-902b-bb6bd326b487	2026-06-23	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Orelli Inc.	4f9f1b4e-8bbb-49b9-8e6c-263edb2c084d	2026-06-22	Warnings	Exact identifier application number: M013
Pain Relief Aspirin Chewable, Low Dose	ASPIRIN	Rite Aid Corporation	65cdce0f-be04-43ba-8c68-bdce7983cfa1	2026-06-22	Warnings	Exact identifier application number: M013
Aspirin Regimen	ASPIRIN	Cardinal Health 110, LLC. DBA Leader	88f425df-712d-4911-824b-94085c7190b6	2026-06-19	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	Meijer Distribution, Inc.	3716a7d4-a555-4e54-aa0a-7b8f3e32addb	2026-06-19	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	DOLGENCORP, LLC	acc94a3e-21b6-4375-9881-38cf9bab8692	2026-06-19	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	L.N.K. International, Inc.	2f6ec676-3832-420e-be91-fce83f6586c8	2026-06-19	Warnings	Exact identifier application number: M013
Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	DOLGENCORP, LLC	e1e24d52-0b4d-400b-8181-e3f6ab75c4f6	2026-06-18	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Oncor Pharmaceuticals	4c396d0e-aa93-4f9e-b065-2e606f7f05cd	2026-06-17	Warnings	Exact identifier application number: M013
LOW DOSE ASPIRIN	ASPIRIN	Famora Inc.	4dc6f119-bbde-db5f-e063-6294a90a9486	2026-06-16	Warnings	Exact identifier application number: M013
Childrens Pain and Fever Relief	ACETAMINOPHEN	Chain Drug Marketing Association, Inc.	420a1e05-caa6-481f-bdab-a670f0220f96	2026-06-16	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	DOLGENCORP, LLC	ce9f4e0d-43fb-499a-b8a2-a997a14841c4	2026-06-16	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	L.N.K. International, Inc.	734cc3d2-6fc5-4dcc-93ed-0b57c1f01345	2026-06-15	Warnings	Exact identifier application number: M013
RIGHT REMEDIES EXTRA STRENGTH Pain Relief PM Caplet	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Strive Pharmaceuticals Inc.	2d63671d-cf7c-bbdd-e063-6294a90affef	2026-06-15	Warnings	Exact identifier application number: M013
TYLENOL Extra Strength	ACETAMINOPHEN	Kenvue Brands LLC	59773893-09a8-47a2-943a-e9ea9da4458a	2026-06-15	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	Shield Pharmaceuticals Corp.	96eb7f9f-ff2d-4661-bbe6-1860aafe03f6	2026-06-15	Warnings	Exact identifier application number: M013
Duralgina Extra Strength	ACETAMINOPHEN	Menper Distributors, Inc.	544e3d7e-a759-384f-e063-6294a90a5baa	2026-06-15	Warnings	Exact identifier application number: M013
pain relief childrens	ACETAMINOPHEN	Rite Aid Corporation	be2286a1-946b-4bf5-b14c-8e86da669594	2026-06-15	Warnings	Exact identifier application number: M013
Aspirin 81	ASPIRIN	Amerisource Bergen	4491faca-f30b-4eb0-bea9-f518f6b2f095	2026-06-15	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
41728CY7UX	MAGNESIUM SALICYLATE	18917-95-8	MAGNESIUM SALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198742	magnesium salicylate 580 MG Oral Tablet	PSN	e5563a0a-776a-83d4-e053-2a95a90a9500	5
198742	magnesium salicylate 580 MG Oral Tablet	SCD	e5563a0a-776a-83d4-e053-2a95a90a9500	5
198742	magnesium salicylate 580 MG (as magnesium salicylate anhydrous 467 MG) Oral Tablet	SY	e5563a0a-776a-83d4-e053-2a95a90a9500	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
47682-074-36	47682007436	75 PACKET in 1 BOX (47682-074-36) / 2 TABLET, FILM COATED in 1 PACKET	75 packet	2022-12-12	0000-00-00	No	No	Current
47682-074-80	47682007480	40 PACKET in 1 BOX (47682-074-80) / 2 TABLET, FILM COATED in 1 PACKET (47682-074-99)	40 packet	2022-09-26	0000-00-00	No	No	Current
47682-074-99	47682007499	2 TABLET, FILM COATED in 1 PACKET (47682-074-99)		2022-09-26		No	No	Current