theraflu expressmax daytime nighttime value pack

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl and acetaminophen, diphenhydramine hcl, phenylephrine hcl

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

Drug Facts

Product Profile

Brand Name theraflu expressmax daytime nighttime value pack
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl and acetaminophen, diphenhydramine hcl, phenylephrine hcl
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-8125
Product ID 0067-8125_15beba82-bd3d-a666-e063-6394a90a8867
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2015-07-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00678125
Hyphenated Format 0067-8125

Supplemental Identifiers

RxCUI
1113705 1298348 1803669

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 expressmax daytime nighttime value pack (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl and acetaminophen, diphenhydramine hcl, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 30 ml
  • 650 mg
  • 20 mg
  • 10 mg
  • 25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0067-8125-16) * 245.5 mL in 1 BOTTLE (0067-8127-08) * 245.5 mL in 1 BOTTLE (0067-8129-08)
source: ndc

Packages (1)

0067-8125-16 1 KIT in 1 CARTON (0067-8125-16) * 245.5 mL in 1 BOTTLE (0067-8127-08) * 245.5 mL in 1 BOTTLE (0067-8129-08)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Theraflu ExpressMax Daytime Nighttime Value Pack ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "15beba82-bd3d-a666-e063-6394a90a8867", "openfda": {"rxcui": ["1113705", "1298348", "1803669"], "spl_set_id": ["9736ad4c-8c2e-421f-b023-f91b72d2828b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0067-8125-16)  *  245.5 mL in 1 BOTTLE (0067-8127-08)  *  245.5 mL in 1 BOTTLE (0067-8129-08)", "package_ndc": "0067-8125-16", "marketing_start_date": "20150715"}], "brand_name": "Theraflu ExpressMax Daytime Nighttime Value Pack", "product_id": "0067-8125_15beba82-bd3d-a666-e063-6394a90a8867", "dosage_form": "KIT", "product_ndc": "0067-8125", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl and Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu ExpressMax", "brand_name_suffix": "Daytime Nighttime Value Pack", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150715", "listing_expiration_date": "20261231"}