Acetaminophen

Product NDC: 69842-491
11-digit product format: 698420491
Labeler code: 69842
Product ID: 69842-491_46547277-f128-b9e7-e063-6294a90a2ccd
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: CVS PHARMACY, INC
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-07-26
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Acetaminophen
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	500 mg/1

Harmonized Identifiers#

Field, Values table
Field	Values
Unii	362O9ITL9D

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69842-491-40	2023-03-02	C162847	48780-1	f386c64a-27c7-0266-e053-dadaa90a7c1a	Rapid Release Gelcaps EXTRA STRENGTH Acetaminophen Gelcaps USP, 500 mg Pain reliever; Fever reducer Aspirin free
69842-491-40	2023-01-30	C162847	48780-1	f386c64a-27c7-0266-e053-dadaa90a7c1a	Rapid Release Gelcaps EXTRA STRENGTH Acetaminophen Gelcaps USP, 500 mg Pain reliever; Fever reducer Aspirin free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69842-491-40	Acetaminophen	400 in 1 BOTTLE	TABLET	400		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69842-491	ACETAMINOPHEN TABLET [CVS PHARMACY, INC]	6	Current NDC, Legacy NDC, 1 package rows	20250504_c2c6d6a1-b492-506d-e053-2995a90aac23.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69842-491-40	69842049140	400 TABLET in 1 BOTTLE (69842-491-40)	400 tablet	2021-07-26	0000-00-00	No	No	Current