tylenol extra strength

Generic: acetaminophen

Labeler: kenvue brands llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tylenol extra strength
Generic Name acetaminophen
Labeler kenvue brands llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 50580-472
Product ID 50580-472_21c39261-4b98-bc43-e063-6394a90a4eb8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-03-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50580472
Hyphenated Format 50580-472

Supplemental Identifiers

RxCUI
198440 209459
UPC
0300450406026
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 tylenol 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 in 1 CARTON (50580-472-01) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (50580-472-02) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (50580-472-03) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (50580-472-04) / 200 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (4)

50580-472-01 1 BOTTLE in 1 CARTON (50580-472-01) / 24 TABLET, FILM COATED in 1 BOTTLE 50580-472-02 1 BOTTLE in 1 CARTON (50580-472-02) / 50 TABLET, FILM COATED in 1 BOTTLE 50580-472-03 1 BOTTLE in 1 CARTON (50580-472-03) / 100 TABLET, FILM COATED in 1 BOTTLE 50580-472-04 1 BOTTLE in 1 CARTON (50580-472-04) / 200 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Tylenol Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21c39261-4b98-bc43-e063-6394a90a4eb8", "openfda": {"upc": ["0300450406026"], "unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["0c5fdda8-5049-46de-e063-6294a90a592b"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-01", "marketing_start_date": "20240318"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-02)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-02", "marketing_start_date": "20240318"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-03)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-03", "marketing_start_date": "20240318"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-04)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-04", "marketing_start_date": "20240318"}], "brand_name": "Tylenol Extra Strength", "product_id": "50580-472_21c39261-4b98-bc43-e063-6394a90a4eb8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50580-472", "generic_name": "Acetaminophen", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tylenol Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240318", "listing_expiration_date": "20261231"}