theraflu severe cold relief combo pack

Generic: acetaminophen, dextromethorphan hbr, diphenhydramine hcl

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name theraflu severe cold relief combo pack
Generic Name acetaminophen, dextromethorphan hbr, diphenhydramine hcl
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-0122
Product ID 0067-0122_f147d82e-4429-4c7b-bd2b-e21a09f21c92
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-04-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00670122
Hyphenated Format 0067-0122

Supplemental Identifiers

RxCUI
2670598 2670677 2679420 2679425 2679426

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 theraflu severe cold relief combo pack (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, diphenhydramine hcl (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 20 mg
  • 650 mg
  • 25 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE, COMBINATION (0067-0122-01) * 6 PACKET in 1 CARTON (0067-0100-06) / 1 POWDER, FOR SOLUTION in 1 PACKET * 6 PACKET in 1 CARTON (0067-0101-06) / 1 POWDER, FOR SOLUTION in 1 PACKET
source: ndc

Packages (1)

0067-0122-01 1 KIT in 1 PACKAGE, COMBINATION (0067-0122-01) * 6 PACKET in 1 CARTON (0067-0100-06) / 1 POWDER, FOR SOLUTION in 1 PACKET * 6 PACKET in 1 CARTON (0067-0101-06) / 1 POWDER, FOR SOLUTION in 1 PACKET

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Theraflu Severe Cold Relief Combo Pack ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "f147d82e-4429-4c7b-bd2b-e21a09f21c92", "openfda": {"rxcui": ["2670598", "2670677", "2679420", "2679425", "2679426"], "spl_set_id": ["f147d82e-4429-4c7b-bd2b-e21a09f21c92"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0067-0122-01)  *  6 PACKET in 1 CARTON (0067-0100-06)  / 1 POWDER, FOR SOLUTION in 1 PACKET *  6 PACKET in 1 CARTON (0067-0101-06)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-0122-01", "marketing_start_date": "20240415"}], "brand_name": "Theraflu Severe Cold Relief Combo Pack", "product_id": "0067-0122_f147d82e-4429-4c7b-bd2b-e21a09f21c92", "dosage_form": "KIT", "product_ndc": "0067-0122", "generic_name": "acetaminophen, dextromethorphan hbr, diphenhydramine hcl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu", "brand_name_suffix": "Severe Cold Relief Combo Pack", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240415", "listing_expiration_date": "20261231"}