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	2026-10-15
excluded package	package	47682-074	47682-074-33	D	Discontinued by firm	2026-10-15
excluded package	package	47682-074	47682-074-99	D	Discontinued by firm	2026-10-15

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 46 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
RIGHT REMEDIES LOW DOSE Aspirin 81mg	ASPIRIN	Strive Pharmaceuticals Inc.	322c0e50-cf75-51ab-e063-6294a90a9235	2025-04-14	Warnings	Exact identifier application number: M013
Bayer Aspirin Regimen Chewable Low Dose Aspirin Orange	ASPIRIN	Bayer HealthCare LLC.	0c6ae05f-760f-34d1-e054-00144ff88e88	2025-04-11	Warnings	Exact identifier application number: M013
Arthriten Inflammatory Pain Formula	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Kobayashi Healthcare International, Inc	c280ca89-4fb5-4050-90ee-d706a550a1ef	2025-04-11	Warnings	Exact identifier application number: M013
Bayer Back and Body Extra Strength	ASPIRIN,CAFFEINE	Bayer HealthCare LLC.	0c77c484-6caf-12ca-e054-00144ff88e88	2025-04-10	Warnings	Exact identifier application number: M013
Adult Low Dose Enteric Coated Aspirin	ASPIRIN	NuCare Pharmaceuticals, Inc.	324937c3-c558-bc79-e063-6294a90acc8e	2025-04-08	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN 500MG	CVS Pharmacy, Inc.	1fde6487-6682-99a3-e063-6294a90a3670	2025-04-04	Warnings	Exact identifier application number: M013
Childrens Acetaminophen	ACETAMINOPHEN	Bryant Ranch Prepack	bdc466c9-d9ae-4293-b7ea-46fb517661c6	2025-04-01	Warnings	Exact identifier application number: M013
Adult Low Dose Enteric Coated Aspirin	ASPIRIN	Geri-Care Pharmaceutical Corp	e327a52a-0e31-44b7-9823-7f60d070ae52	2025-04-01	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Proficient Rx LP	9af5ccc8-aac0-4339-a9f6-58fdc9b91c57	2025-04-01	Warnings	Exact identifier application number: M013
ASPIRIN 325 MG EC	ASPIRIN	Bryant Ranch Prepack	9d0449d2-c0c6-4e74-931b-35dc62584028	2025-03-31	Warnings	Exact identifier application number: M013
Aspirin 81 mg	ASPIRIN	Bryant Ranch Prepack	cce1e8bd-63c8-403a-bc32-e6788493f604	2025-03-31	Warnings	Exact identifier application number: M013
Adwe Feverx Acetaminophen Caplets, 500 mg Extra Strength	ACETAMINOPHEN	Aurex Laboratories Limited Liability Company	948c5826-6f35-484d-bb3f-cecf6a4b5c13	2025-03-31	Warnings	Exact identifier application number: M013
Infants Pain and Fever	ACETAMINOPHEN	WALGREENS	281a530b-c759-50eb-e063-6394a90abb4f	2025-03-28	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	WR Group, Inc.	8281771c-485c-42a9-9a1c-9a7a4298c5b8	2025-03-28	Warnings	Exact identifier application number: M013
Acetaminophen Regular strength	ACETAMINOPHEN	PD-Rx Pharmaceuticals, Inc.	4181efc2-d183-410c-b647-233444c57e32	2025-03-20	Warnings	Exact identifier application number: M013
CounterAct Pain	ACETAMINOPHEN	Melaleuca, Inc.	7faf76b4-7f25-377d-e053-2a91aa0a19d4	2025-03-20	Boxed warning, Warnings	Exact identifier application number: M013
Mejoral	ACETAMINOPHEN, CAFFEINE	OPMX LLC	0bccf571-fcb9-2dd5-e063-6294a90a5f16	2025-03-19	Warnings	Exact identifier application number: M013
ARTRIFIN 24 CAPLETS	ACETAMINOPHEN, ASPIRIN, CAFFEINE	OPMX LLC	e7f15c2b-a730-b54f-e053-2a95a90a3b3e	2025-03-19	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	TARGET Corporation	1fc3806e-a5c4-4a6e-951b-dfbf9f5771f1	2025-03-17	Warnings	Exact identifier application number: M013
Signature Select Effervescent Pain Relief	ASPIRIN	Safeway Inc.	304fca65-2867-c963-e063-6394a90a183f	2025-03-14	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