Pain Relief Aspirin

Product NDC: 11822-2180
Requested package NDC: 11822-2180-9
11-digit product format: 118222180
Labeler code: 11822
Product ID: 11822-2180_bf297166-0b88-4929-ab29-76fcf0b1ae6b
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: Rite Aid Corporation
Application: part343
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 1990-09-12
Marketing end: 0000-00-00
Substance: ASPIRIN
Active strength: 81 mg/1
Pharmacologic classes: Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
NDC exclude flag: No
Listing certified through: 2023-12-31
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	11822-2180	11822-2180-9	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 1 · 2 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	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11822-2180	11822-2180-9	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11822-2180	11822-2180-9	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID]	11
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID]	11
DEXTRATES	INACTIVE INGREDIENT	G263MI44RU	PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID]	11
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID]	11
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, CHEWABLE [RITE AID]	11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-2180	PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, CHEWABLE [RITE AID CORPORATION]	24	Legacy NDC	20250312_77cfa372-e3ad-4112-bbd1-5227342aaafd.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
R16CO5Y76E	ASPIRIN	50-78-2	ASPIRIN

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-2180-9	11822218009	3 BOTTLE, PLASTIC in 1 CARTON (11822-2180-9) > 36 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC	1990-09-12	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Rite Aid 44-218A-Delisted	Rite Aid Corporation \| LNK International, Inc.	2025-03-10	HUMAN OTC DRUG LABEL	24