Pain Relief

Product NDC: 11822-0812
11-digit product format: 118220812
Labeler code: 11822
Product ID: 11822-0812_c301fedd-e98d-481b-8749-4156bb8383e5
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Rite Aid Corporation
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1993-04-02
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 6 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	11822-0812	11822-0812-1	D	Discontinued by firm	2026-10-05
excluded package	package	11822-0812	11822-0812-3	D	Discontinued by firm	2026-10-05
excluded package	package	11822-0812	11822-0812-4	D	Discontinued by firm	2026-10-05
excluded package	package	11822-0812	11822-0812-5	D	Discontinued by firm	2026-10-05
excluded package	package	11822-0812	11822-0812-6	D	Discontinued by firm	2026-10-05
excluded package	package	11822-0812	11822-0812-8	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 2 · 61 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	11822-0812-5	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11822-0812-4	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11822-0812-3	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11822-0812-1	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11822-0812-6	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	11822-0812-8	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	11822-0812-6	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11822-0812-3	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11822-0812-8	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11822-0812-5	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11822-0812-1	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	11822-0812-4	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	11822-0812-6	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11822-0812-3	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11822-0812-8	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11822-0812-5	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11822-0812-1	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	11822-0812-4	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	11822-0812-6	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11822-0812-3	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11822-0812-8	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11822-0812-5	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11822-0812-1	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	11822-0812-4	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	11822-0812-6	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11822-0812-3	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11822-0812-8	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11822-0812-5	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11822-0812-1	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	11822-0812-4	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	11822-0812-6	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11822-0812-3	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11822-0812-8	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11822-0812-5	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11822-0812-1	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	11822-0812-4	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	11822-0812-6	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11822-0812-3	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11822-0812-8	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11822-0812-5	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11822-0812-1	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	11822-0812-4	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	11822-0812-6	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11822-0812-3	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11822-0812-8	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11822-0812-5	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	11822-0812-4	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	11822-0812-6	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11822-0812-3	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11822-0812-8	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11822-0812-5	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	11822-0812-4	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	11822-0812-6	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	11822-0812-3	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	11822-0812-8	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	11822-0812-4	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	11822-0812-6	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	11822-0812-3	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	11822-0812-8	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	11822-0812-6	`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 Relief
Brand name suffix: Extra Strength
Listing expiration: 2027-12-31

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
d846065a-5c39-4f4b-894c-4280acaaf4fa	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11822-0812-1	Pain ReliefExtra Strength	100 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	100	25
11822-0812-1	Pain ReliefExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	25
11822-0812-2	Pain ReliefExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	25
11822-0812-2	Pain ReliefExtra Strength	12 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	12	25
11822-0812-3	Pain ReliefExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	25
11822-0812-3	Pain ReliefExtra Strength	2 in 1 BLISTER PACK	TABLET, FILM COATED	2	25
11822-0812-4	Pain ReliefExtra Strength	500 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	500	25
11822-0812-5	Pain ReliefExtra Strength	50 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	50	25
11822-0812-5	Pain ReliefExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	25
11822-0812-6	Pain ReliefExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	25
11822-0812-6	Pain ReliefExtra Strength	16 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	16	25
11822-0812-8	Pain ReliefExtra Strength	24 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	24	25
11822-0812-8	Pain ReliefExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	25

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9
CASTOR OIL	INACTIVE INGREDIENT	D5340Y2I9G	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID]	9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-0812	PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID CORPORATION]	24	Current NDC, Legacy NDC, 13 package rows	20240911_d846065a-5c39-4f4b-894c-4280acaaf4fa.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 1 of 83 · 1,657 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
childrens fever reducer and pain reliever	ACETAMINOPHEN	Rite Aid Corporation	7f445de3-30cf-4bd8-892d-05979cd399e7	2026-09-09	Warnings	Exact identifier application number: M013
Low Dose Aspirin	ASPIRIN	Strategic Sourcing Services LLC	7ce4807e-7bd5-41f1-a9c7-1f3af6acdc09	2026-09-09	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	Wal-Mart Stores Inc	78874258-16cc-40b5-9e15-5943eddfce94	2026-09-08	Warnings	Exact identifier application number: M013
Pain and Fever Childrens	ACETAMINOPHEN	DOLGENCORP, LLC	c637b39c-a049-43af-a582-fc242e940d85	2026-09-08	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	Walgreen Company	f7667529-09c0-4603-8080-f236144fac36	2026-09-08	Warnings	Exact identifier application number: M013
UP AND UP CHILDRENS ACETAMINOPHEN	ACETAMINOPHEN	Target Corporation	e2989ead-7fdc-4295-bf94-423195775670	2026-09-08	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	Rite Aid Corporation	d846065a-5c39-4f4b-894c-4280acaaf4fa	2026-09-08	Warnings	Exact identifier application number: M013 ndc (product): 11822-0812
DESENFRIOL-ITO PLUS	ACETAMINOPHEN	OPMX LLC	5ac41edd-e845-734d-e063-6294a90a990a	2026-09-05	Warnings	Exact identifier application number: M013
DRX CHOICE Regular Strength	ACETAMINOPHEN	Raritan Pharmaceuticals Inc.	8bacb24a-24d0-4175-b3e0-05efb5f5d373	2026-09-05	Warnings	Exact identifier application number: M013
Mejoralito	ACETAMINOPHEN	OPMX	5a963a92-e29d-05ba-e063-6394a90a3a47	2026-09-03	Warnings	Exact identifier application number: M013
Pentrexcilina	ACETAMINOPHEN	OPMX LLC	5a98e123-8e28-6732-e063-6394a90a010c	2026-09-03	Warnings	Exact identifier application number: M013
infants pain and fever	ACETAMINOPHEN	CVS Pharmacy	53b06c48-598e-41ad-ac7a-5508c195535c	2026-09-03	Warnings	Exact identifier application number: M013
Aspirin Regular Strength	ASPIRIN	Cardinal Health 110, LLC. DBA Leader	2777beea-06d7-4ff5-ae4a-ad7a117dfb62	2026-09-02	Warnings	Exact identifier application number: M013
AMAZON BASIC CARE ACETAMINOPHEN	ACETAMINOPHEN	Amazon.com Services LLC	113d92bf-f6c9-cc3d-e063-6294a90af033	2026-09-02	Warnings	Exact identifier application number: M013
Extra Strength Pain Reliever	ACETAMINOPHEN	Shield Pharmaceuticals Corp.	78052120-40d8-4a3f-b72f-cc78ca76213b	2026-09-02	Warnings	Exact identifier application number: M013
Adult Low Dose Chewable Aspirin	ASPIRIN	Farmacias De Similares TX LLC	513ea306-74c6-96e3-e063-6394a90a8262	2026-09-01	Warnings	Exact identifier application number: M013
Kroger Children Pain plus Fever chewables	ACETAMINOPHEN	KROGER COMPANY	83b5733c-70a1-4383-9729-2eb896d0149a	2026-09-01	Warnings	Exact identifier application number: M013
Pain Reliever PM Extra Strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	TOP CARE (Topco Associates LLC)	923b443d-73cc-4c52-92e4-a075786b1ae3	2026-09-01	Warnings	Exact identifier application number: M013
ACETAMINOPHEN PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Amazon.com Services LLC	99a137d6-07eb-43bc-b4b4-1a23041d595e	2026-08-31	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	CVS PHARMACY	64a1ebe7-af28-4b09-96e8-28fa4dcc52bd	2026-08-31	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	d846065a-5c39-4f4b-894c-4280acaaf4fa	25
198440	acetaminophen 500 MG Oral Tablet	SCD	d846065a-5c39-4f4b-894c-4280acaaf4fa	25
198440	APAP 500 MG Oral Tablet	SY	d846065a-5c39-4f4b-894c-4280acaaf4fa	25

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-0812-1	11822081201	1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-1) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC		1993-04-02	0000-00-00	No	No	Current
11822-0812-2	11822081202	1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-2) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC		1993-04-02	0000-00-00	No	No	Current
11822-0812-3	11822081203	1 BLISTER PACK in 1 CARTON (11822-0812-3) > 2 TABLET, FILM COATED in 1 BLISTER PACK	1 blister pack	1993-04-02	0000-00-00	No	No	Current
11822-0812-4	11822081204	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-0812-4)		1993-04-02	0000-00-00	No	No	Current
11822-0812-5	11822081205	1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-5) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC		1993-04-02	0000-00-00	No	No	Current
11822-0812-6	11822081206	1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-6) > 16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC		1993-04-02	2021-10-08	No	No	Current
11822-0812-8	11822081208	1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-8) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC		1993-04-02	0000-00-00	No	No	Current