acetaminophen extra strength

Generic: acetaminophen

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler cvs pharmacy
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
CVS PHARMACY

Identifiers & Regulatory

Product NDC 69842-931
Product ID 69842-931_0e241bc2-95ca-4bcf-a1ad-faf575c3d6aa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2005-12-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842931
Hyphenated Format 69842-931

Supplemental Identifiers

RxCUI
198440
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name acetaminophen extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (69842-931-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-17)
  • 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-29)
source: ndc

Packages (3)

69842-931-08 1 BOTTLE, PLASTIC in 1 CARTON (69842-931-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 69842-931-17 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-17) 69842-931-29 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-29)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e241bc2-95ca-4bcf-a1ad-faf575c3d6aa", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["64a1ebe7-af28-4b09-96e8-28fa4dcc52bd"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (69842-931-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "69842-931-08", "marketing_start_date": "20051211"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-17)", "package_ndc": "69842-931-17", "marketing_start_date": "20051211"}, {"sample": false, "description": "150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-29)", "package_ndc": "69842-931-29", "marketing_end_date": "20270131", "marketing_start_date": "20051211"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "69842-931_0e241bc2-95ca-4bcf-a1ad-faf575c3d6aa", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69842-931", "generic_name": "Acetaminophen", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20051211", "listing_expiration_date": "20261231"}