Pain Relief

Product NDC: 53943-304
11-digit product format: 539430304
Labeler code: 53943
Product ID: 53943-304_288998e3-a490-9c47-e063-6394a90ae9aa
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET, COATED
Route: ORAL
Labeler: DISCOUNT DRUG MART
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-01-05
Substance: ACETAMINOPHEN
Active strength: 500 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 package	package	53943-304	53943-304-02	D	Discontinued by firm	2026-10-20
excluded package	package	53943-304	53943-304-04	D	Discontinued by firm	2026-10-20
excluded package	package	53943-304	53943-304-09	D	Discontinued by firm	2026-10-20

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 · 18 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	53943-304-04	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	53943-304-02	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	53943-304-09	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	53943-304-04	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	53943-304-02	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	53943-304-09	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	53943-304-04	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	53943-304-02	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	53943-304-09	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	53943-304-04	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	53943-304-02	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	53943-304-09	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	53943-304-04	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	53943-304-02	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	53943-304-09	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	53943-304-04	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	53943-304-02	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	53943-304-09	`cdf11ea48f46…`	`ba0047e9e063…`

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: Pain Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
362O9ITL9D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198440	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
972f09a7-2aa1-4b1b-a6dc-2c4578a07803	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
53943-304-02	Pain Relief	50 in 1 BOTTLE, PLASTIC	TABLET, COATED	50	5
53943-304-02	Pain Relief	1 in 1 CARTON	TABLET, COATED	1	5
53943-304-04	Pain Relief	1 in 1 CARTON	TABLET, COATED	1	5
53943-304-04	Pain Relief	100 in 1 BOTTLE, PLASTIC	TABLET, COATED	100	5
53943-304-06	Pain Relief	500 in 1 BOTTLE, PLASTIC	TABLET, COATED	500	5
53943-304-09	Pain Relief	100 in 1 BOTTLE, PLASTIC	TABLET, COATED	100	5
53943-304-09	Pain Relief	2 in 1 CARTON	TABLET, COATED	2	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53943-304	PAIN RELIEF (ACETAMINOPHEN) TABLET, COATED [DISCOUNT DRUG MART]	5	Current NDC, Legacy NDC, 7 package rows	20241208_972f09a7-2aa1-4b1b-a6dc-2c4578a07803.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 20 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Excedrin Rapid Relief	ACETAMINOPHEN	Haleon US Holdings LLC	3a36b7ca-396e-cfd8-e063-6294a90a76ab	2026-02-22	Warnings	Exact identifier application number: M013
CHILDRENS Acetaminophen	CHILDRENS ACETAMINOPHEN	Kesin Pharma Corporation	4af5b025-1fd7-e825-e063-6294a90aa005	2026-02-16	Warnings	Exact identifier application number: M013
Infants TYLENOL	ACETAMINOPHEN	Kenvue Brands LLC	4a121a53-dbae-05c7-e063-6294a90aed89	2026-02-13	Warnings	Exact identifier application number: M013
MAX relief junior Grape	CHILDRENS ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	562d7901-44d6-4d9b-be8b-a8d468a22c43	2026-02-13	Warnings	Exact identifier application number: M013
acetaminophen	ACETAMINOPHEN	Major Pharmaceuticals	020fa486-31f0-4e0c-84d3-5b3aaded1eeb	2026-02-13	Warnings	Exact identifier application number: M013
ASPIRIN Low Strength	ASPIRIN	CVS Pharmacy	6e1c1129-562b-4a8a-ac37-db3cb2a82735	2026-02-11	Warnings	Exact identifier application number: M013
CVS Acetaminophen	ACETAMINOPHEN	CVS Pharmacy	3dd21aaf-13b2-9e81-e063-6294a90afaec	2026-02-11	Warnings	Exact identifier application number: M013
Pain Relief PM	ACETAMINOPHEN, ASPIRIN, DIPHENHYDRAMINE CITRATE	CVS Pharmacy	ddd78b28-6e10-4708-bed1-8aea087b3d82	2026-02-11	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	Topco Associates, LLC	2e31fe65-5f50-455b-99fa-c72879f43545	2026-02-10	Warnings	Exact identifier application number: M013
Pain Relief Childrens	ACETAMINOPHEN	Amerisource Bergen	9ea8bb1f-1924-4430-98bd-f2674d0da748	2026-02-09	Warnings	Exact identifier application number: M013
Acetaminophen , Caffeine and pyrilamine maleate	ACETAMINOPHEN , CAFFEINE AND PYRILAMINE MALEATE	Softgel Healthcare Pvt Ltd	4a61313e-1b48-29df-e063-6394a90a27f0	2026-02-09	Warnings	Exact identifier application number: M013
good sense aspirin	ASPIRIN	L. Perrigo Company	e9fddbc1-11fe-4cf6-8794-1650fa1b32ae	2026-02-07	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Chain Drug Marketing Association, Inc.	2d375ec9-a528-4048-a15b-652fa20e74a7	2026-02-06	Warnings	Exact identifier application number: M013
Adult Low Dose Enteric Coated Aspirin	ASPIRIN	Sportpharm LLC	d3379569-7949-4f78-b634-5d4178b21ea4	2026-02-06	Warnings	Exact identifier application number: M013
Buffered Aspirin	ASPIRIN	Cardinal Health 110, LLC. DBA Leader	e5f68c1a-21f3-45a1-861f-229a95b3721c	2026-02-06	Warnings	Exact identifier application number: M013
pain relief extra strength	ACETAMINOPHEN	HyVee Inc	1e707628-08b1-4c72-b71c-2b4ae96071f2	2026-02-06	Warnings	Exact identifier application number: M013
CareOne Acetaminophen PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	American Sales Company	2d2ded37-f241-4976-886d-5c038a85bfe1	2026-02-05	Warnings	Exact identifier application number: M013
Dolex Fem	ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE	Pharmadel LLC	b1cab10b-19f1-f5d5-e053-2995a90a4d5f	2026-02-05	Warnings	Exact identifier application number: M013
Alka-Seltzer Extra Strength Pain Relief	ANHYDROUS CITRIC ACID, ASPIRIN	Bayer HealthCare LLC.	4a16b6e5-f0c6-e3a4-e063-6294a90a85ad	2026-02-05	Warnings	Exact identifier application number: M013
Pain Relief childrens	ACETAMINOPHEN	CVS PHARMACY	b8ab85a6-3eab-4ef4-a13d-5ac300480f63	2026-02-03	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	972f09a7-2aa1-4b1b-a6dc-2c4578a07803	5
198440	acetaminophen 500 MG Oral Tablet	SCD	972f09a7-2aa1-4b1b-a6dc-2c4578a07803	5
198440	APAP 500 MG Oral Tablet	SY	972f09a7-2aa1-4b1b-a6dc-2c4578a07803	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
53943-304-02	53943030402	1 BOTTLE, PLASTIC in 1 CARTON (53943-304-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC	2010-01-05	0000-00-00	No	No	Current
53943-304-04	53943030404	1 BOTTLE, PLASTIC in 1 CARTON (53943-304-04) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC	2010-03-04	0000-00-00	No	No	Current
53943-304-06	53943030406	500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-304-06)	2010-01-05	0000-00-00	No	No	Current
53943-304-09	53943030409	2 BOTTLE, PLASTIC in 1 CARTON (53943-304-09) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC	2013-04-04	0000-00-00	No	No	Current