extra strength tylenol cold plus flu multi-action day/night

Generic: acetaminophen, pseudoephedrine hydrochloride, dextromethorphan hydrobromide, and chlorpheniramine maleate

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

Drug Facts

Product Profile

Brand Name extra strength tylenol cold plus flu multi-action day/night
Generic Name acetaminophen, pseudoephedrine hydrochloride, dextromethorphan hydrobromide, and chlorpheniramine maleate
Labeler kenvue brands llc
Dosage Form KIT
Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 50580-374
Product ID 50580-374_21719087-b7ff-e583-e063-6394a90aa10c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-06-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50580374
Hyphenated Format 50580-374

Supplemental Identifiers

RxCUI
1089968 1250743 2558505
UPC
0300450149244

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 extra strength tylenol cold plus flu multi-action day/night (source: ndc)
Generic Name acetaminophen, pseudoephedrine hydrochloride, dextromethorphan hydrobromide, and chlorpheniramine maleate (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 15 mg
  • 30 mg
  • 2 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE (50580-374-01) * 2 BLISTER PACK in 1 CARTON / 8 TABLET, FILM COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

50580-374-01 1 KIT in 1 PACKAGE (50580-374-01) * 2 BLISTER PACK in 1 CARTON / 8 TABLET, FILM COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Extra Strength TYLENOL Cold plus Flu Multi-Action Day/Night ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "21719087-b7ff-e583-e063-6394a90aa10c", "openfda": {"upc": ["0300450149244"], "rxcui": ["1089968", "1250743", "2558505"], "spl_set_id": ["712ba011-79aa-469b-9f0f-04a0b4b705bd"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (50580-374-01)  *  2 BLISTER PACK in 1 CARTON / 8 TABLET, FILM COATED in 1 BLISTER PACK *  2 BLISTER PACK in 1 CARTON / 4 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-374-01", "marketing_start_date": "20210621"}], "brand_name": "Extra Strength TYLENOL Cold plus Flu Multi-Action Day/Night", "product_id": "50580-374_21719087-b7ff-e583-e063-6394a90aa10c", "dosage_form": "KIT", "product_ndc": "50580-374", "generic_name": "acetaminophen, pseudoephedrine hydrochloride, dextromethorphan hydrobromide, and chlorpheniramine maleate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength TYLENOL Cold plus Flu Multi-Action", "brand_name_suffix": "Day/Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210621", "listing_expiration_date": "20261231"}