theraflu severe cold relief daytime and theraflu severe cold relief nighttime

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl, 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 daytime and theraflu severe cold relief nighttime
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl, diphenhydramine hcl
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-6804
Product ID 0067-6804_103fee61-db67-5ad2-e063-6394a90a572a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-01-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00676804
Hyphenated Format 0067-6804

Supplemental Identifiers

RxCUI
1189316 1659960 2640034

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 daytime and theraflu severe cold relief nighttime (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl, diphenhydramine hcl (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 20 mg
  • 10 mg
  • 650 mg
  • 25 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE, COMBINATION (0067-6804-02) * 6 PACKET in 1 CARTON (0067-6802-02) / 237 mL in 1 PACKET * 6 PACKET in 1 CARTON (0067-6803-02) / 237 mL in 1 PACKET
source: ndc

Packages (1)

0067-6804-02 1 KIT in 1 PACKAGE, COMBINATION (0067-6804-02) * 6 PACKET in 1 CARTON (0067-6802-02) / 237 mL in 1 PACKET * 6 PACKET in 1 CARTON (0067-6803-02) / 237 mL in 1 PACKET

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Theraflu Severe Cold Relief Daytime and Theraflu Severe Cold Relief Nighttime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "103fee61-db67-5ad2-e063-6394a90a572a", "openfda": {"rxcui": ["1189316", "1659960", "2640034"], "spl_set_id": ["e5ef7b85-feee-44a7-bd0e-ed91352c7434"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0067-6804-02)  *  6 PACKET in 1 CARTON (0067-6802-02)  / 237 mL in 1 PACKET *  6 PACKET in 1 CARTON (0067-6803-02)  / 237 mL in 1 PACKET", "package_ndc": "0067-6804-02", "marketing_start_date": "20230120"}], "brand_name": "Theraflu Severe Cold Relief Daytime and Theraflu Severe Cold Relief Nighttime", "product_id": "0067-6804_103fee61-db67-5ad2-e063-6394a90a572a", "dosage_form": "KIT", "product_ndc": "0067-6804", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, Diphenhydramine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold Relief Daytime and Theraflu Severe Cold Relief Nighttime", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230120", "listing_expiration_date": "20261231"}