Pain Reliever

Product NDC: 11822-6440
Requested package NDC: 11822-6440-1
11-digit product format: 118226440
Labeler code: 11822
Product ID: 11822-6440_43ec0026-8447-4aff-959e-6f813eb88005
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: LIQUID
Route: ORAL
Labeler: Rite Aid Corporation
Application: part343
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-01-31
Marketing end: 0000-00-00
Substance: ACETAMINOPHEN
Active strength: 500 mg/15mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	11822-6440	11822-6440-1	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 · 3 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Archive	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	11822-6440	11822-6440-1	I	Inactivated by FDA	excluded / ndc_excluded.zip	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	11822-6440	11822-6440-1	I	Inactivated by FDA	excluded / ndc_excluded.zip	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	11822-6440	11822-6440-1	I	Inactivated by FDA	excluded / ndc_excluded.zip	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11822-6440-1	2023-02-20	C162847	48780-1	d6a99b39-3a8e-a426-e053-dadaa90af4c2	Drug Facts
11822-6440-1	2022-01-28	C162847	48780-1	d6a99b39-3a8e-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11822-6440-1	Pain RelieverExtra Strength	237 mL in 1 BOTTLE, PLASTIC	LIQUID	237		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-6440	PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) LIQUID [RITE AID CORPORATION]	3	Legacy NDC, 1 package rows	20240503_b628a3d1-4534-453c-ac5a-573325662ddc.zip

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-6440-1	11822644001	237 mL in 1 BOTTLE, PLASTIC (11822-6440-1)	237 ml	2020-01-31	0000-00-00	No	No	Current