Pain Reliever

Product NDC: 0363-0519
11-digit product format: 003630519
Labeler code: 0363
Product ID: 0363-0519_47a1e1b6-6aea-4562-8c40-bcf5bfe79e4c
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET, COATED
Route: ORAL
Labeler: Walgreen Company
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2004-05-10
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 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	0363-0519	0363-0519-19	D	Discontinued by firm	2026-10-15
excluded package	package	0363-0519	0363-0519-20	D	Discontinued by firm	2026-10-15
excluded package	package	0363-0519	0363-0519-29	D	Discontinued by firm	2026-10-15
excluded package	package	0363-0519	0363-0519-54	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 · 48 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	0363-0519-54	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0363-0519-20	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0363-0519-19	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	0363-0519-29	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0519-54	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0519-29	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0519-19	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	0363-0519-20	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0519-54	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0519-29	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0519-19	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	0363-0519-20	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0519-54	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0519-29	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0519-19	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	0363-0519-20	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0519-54	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0519-29	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0519-19	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	0363-0519-20	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0519-54	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0519-29	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0519-19	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	0363-0519-20	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	0363-0519-54	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	0363-0519-29	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	0363-0519-19	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	0363-0519-20	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	0363-0519-54	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	0363-0519-29	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	0363-0519-19	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	0363-0519-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	0363-0519-54	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	0363-0519-29	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	0363-0519-19	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	0363-0519-20	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	0363-0519-20	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	0363-0519-29	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	0363-0519-54	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	0363-0519-19	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	0363-0519-20	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	0363-0519-29	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	0363-0519-54	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	0363-0519-19	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	0363-0519-20	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	0363-0519-29	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	0363-0519-54	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	0363-0519-19	`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: Pain Reliever
Brand name suffix: Extra Strength
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
fa33f6ef-522b-4630-9716-92371d9cd24a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0363-0519-08	Pain RelieverExtra Strength	1 in 1 CARTON	TABLET, COATED	1	24
0363-0519-08	Pain RelieverExtra Strength	24 in 1 BOTTLE, PLASTIC	TABLET, COATED	24	24
0363-0519-12	Pain RelieverExtra Strength	100 in 1 BOTTLE, PLASTIC	TABLET, COATED	100	24
0363-0519-12	Pain RelieverExtra Strength	1 in 1 CARTON	TABLET, COATED	1	24
0363-0519-15	Pain RelieverExtra Strength	1 in 1 CARTON	TABLET, COATED	1	24
0363-0519-15	Pain RelieverExtra Strength	50 in 1 BOTTLE, PLASTIC	TABLET, COATED	50	24
0363-0519-19	Pain RelieverExtra Strength	8 in 1 VIAL	TABLET, COATED	8	24
0363-0519-19	Pain RelieverExtra Strength	1 in 1 CARTON	TABLET, COATED	1	24
0363-0519-20	Pain RelieverExtra Strength	225 in 1 BOTTLE, PLASTIC	TABLET, COATED	225	24
0363-0519-20	Pain RelieverExtra Strength	1 in 1 CARTON	TABLET, COATED	1	24
0363-0519-29	Pain RelieverExtra Strength	150 in 1 BOTTLE, PLASTIC	TABLET, COATED	150	24
0363-0519-37	Pain RelieverExtra Strength	1 in 1 CARTON	TABLET, COATED	1	24
0363-0519-37	Pain RelieverExtra Strength	75 in 1 BOTTLE, PLASTIC	TABLET, COATED	75	24
0363-0519-54	Pain RelieverExtra Strength	375 in 1 BOTTLE, PLASTIC	TABLET, COATED	375	24
0363-0519-92	Pain RelieverExtra Strength	150 in 1 BOTTLE, PLASTIC	TABLET, COATED	150	24

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0363-0519-08	EA - Each	0363-0519	9a69870d-fdb2-4bc4-8a04-1bf8f981ae42	1	2012-07-24
0363-0519-12	EA - Each	0363-0519	3e513c0c-aedd-48d9-bcf5-603984d6f238	1	2012-07-24
0363-0519-15	EA - Each	0363-0519	beabd538-bc4f-4d80-a59a-8a7884e49924	1	2012-07-24
0363-0519-19	EA - Each	0363-0519	4dd1144b-a6a2-44da-a280-f0e95c923466	1	2012-07-24
0363-0519-20	EA - Each	0363-0519	ca07599c-a398-4321-be29-e16da39195a1	1	2012-07-24
0363-0519-29	EA - Each	0363-0519	3b4f0f1a-ebe6-4702-ba0b-70a0324c373a	1	2012-07-24
0363-0519-54	EA - Each	0363-0519	68c192ff-03d2-4c02-a129-310a1134b99a	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
D&C RED NO. 33	INACTIVE INGREDIENT	9DBA0SBB0L	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
GELATIN	INACTIVE INGREDIENT	2G86QN327L	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN CO.]	9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0519	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [WALGREEN COMPANY]	23	Current NDC, Legacy NDC, 15 package rows	20250104_fa33f6ef-522b-4630-9716-92371d9cd24a.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 14 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pain Reliever	ACETAMINOPHEN	HHH Pharmaceuticals	0c66b05d-132d-4c79-abfe-415fd68bbb9c	2026-05-06	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Better Living Brands, LLC	5ebd04d8-52c7-4c72-a4c1-fc7fd488ea24	2026-05-06	Warnings	Exact identifier application number: M013
Back and Body Extra Strength	ASPIRIN, CAFFEINE	Cardinal Health 110, LLC. DBA Leader	519eb216-9fa6-4d60-a2a4-3310bdb5b4ab	2026-05-06	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Geiss, Destin & Dunn Inc.	b8f6e486-5332-4c46-ab6c-7de04c91c60b	2026-05-06	Warnings	Exact identifier application number: M013
MAX relief junior Grape	CHILDRENS ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	c60494f0-5a50-41da-bcb4-88178ded54b7	2026-05-05	Warnings	Exact identifier application number: M013
equate pain relief pm	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	WALMART INC.	85129749-c1a7-4c4a-933f-c3c4768e2cdd	2026-05-05	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	ARMY AND AIR FORCE EXCHANGE SERVICE	f3feca65-adc1-469f-bef6-12c860599abe	2026-05-04	Warnings	Exact identifier application number: M013
Childrens Pain and Fever	ACETAMINOPHEN	Strategic Sourcing Services LLC	4dda3534-4e83-447b-be75-33dadce06c47	2026-05-04	Warnings	Exact identifier application number: M013
Aspirin Low Dose Chewable Orange	ASPIRIN	Major Pharmaceuticals	4ba6eed3-004a-4576-b7f7-685fae49cf6a	2026-05-04	Warnings	Exact identifier application number: M013
Back and Body	ASPIRIN, CAFFEINE	Kroger Company	366b58db-1ac3-427b-b42a-5f56a14e298c	2026-05-01	Warnings	Exact identifier application number: M013
Tylenol PM	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Savings Distributors LLC	8ed9a9f0-d37e-5c10-e053-2a95a90a559f	2026-05-01	Warnings	Exact identifier application number: M013
Tylenol Extra Strength	ACETAMINOPHEN	Savings Distributors LLC	8ed90757-833e-f4d9-e053-2995a90a29db	2026-05-01	Warnings	Exact identifier application number: M013
Acetaminophen , Aspirin and Caffeine	ACETAMINOPHEN , ASPIRIN AND CAFFEINE	Softgel Healthcare Pvt Ltd	4543e156-1deb-666e-e063-6394a90a719c	2026-04-27	Warnings	Exact identifier application number: M013
Acetaminophen , Caffeine and pyrilamine maleate	ACETAMINOPHEN , CAFFEINE AND PYRILAMINE MALEATE	Softgel Healthcare Pvt Ltd	45478958-ad86-4d87-e063-6394a90a3c45	2026-04-27	Warnings	Exact identifier application number: M013
Medique at Home Aspirin	ASPIRIN	Sportpharm LLC	0f2aa75e-534f-478b-811e-fb492b7af9bb	2026-04-24	Warnings	Exact identifier application number: M013
Medique at Home APAP Extra Strength	ACETAMINOPHEN 500 MG	Sportpharm LLC	cc280926-ad94-4017-a04a-b4315807eacb	2026-04-24	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Health Pharma USA LLC	503868bb-48e0-b718-e063-6394a90a9c5b	2026-04-24	Warnings	Exact identifier application number: M013
BC CHERRY	ASPIRIN AND CAFFEINE	Medtech Products Inc.	c5fa6660-a549-49ff-ac2b-5799afa22ec5	2026-04-24	Warnings	Exact identifier application number: M013
Doans Maximum Strength	MAGNESIUM SALICYLATE	Dr. Reddy's Laboratories Inc.	c906df41-bb45-03ea-b1a8-2b9816d55c97	2026-04-24	Warnings	Exact identifier application number: M013
Extra Strength Acetaminophen	ACETAMINOPHEN	TIME CAP LABORATORIES, INC.	48912649-9fa1-a11f-e063-6294a90a8a72	2026-04-23	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	fa33f6ef-522b-4630-9716-92371d9cd24a	24
198440	acetaminophen 500 MG Oral Tablet	SCD	fa33f6ef-522b-4630-9716-92371d9cd24a	24
198440	APAP 500 MG Oral Tablet	SY	fa33f6ef-522b-4630-9716-92371d9cd24a	24

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0519-08	00363051908	1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-08) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC		2004-05-10	0000-00-00	No	No	Current
0363-0519-12	00363051912	1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-12) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC		2004-05-10	0000-00-00	No	No	Current
0363-0519-15	00363051915	1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-15) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC		2004-05-10	0000-00-00	No	No	Current
0363-0519-19	00363051919	8 in 1 VIAL						Historical
0363-0519-20	00363051920	1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-20) > 225 TABLET in 1 BOTTLE, PLASTIC		2004-05-10	0000-00-00	No	No	Current
0363-0519-29	00363051929	150 TABLET in 1 BOTTLE (0363-0519-29)	150 tablet	2004-05-10	0000-00-00	No	No	Current
0363-0519-37	00363051937	1 BOTTLE, PLASTIC in 1 CARTON (0363-0519-37) / 75 TABLET, COATED in 1 BOTTLE, PLASTIC		2024-12-30		No	No	Current
0363-0519-54	00363051954	375 TABLET in 1 BOTTLE, PLASTIC (0363-0519-54)	375 tablet	2004-05-10	0000-00-00	No	No	Current
0363-0519-92	00363051992	150 TABLET, COATED in 1 BOTTLE, PLASTIC (0363-0519-92)		2004-05-10	0000-00-00	No	No	Current