theraflu flu relief maximum strength daytime nighttime combo pack

Generic: acetaminophen, dextromethorphan hbr and acetaminophen, chlorpheniramine maleate, dextromethorphan hbr

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

Drug Facts

Product Profile

Brand Name theraflu flu relief maximum strength daytime nighttime combo pack
Generic Name acetaminophen, dextromethorphan hbr and acetaminophen, chlorpheniramine maleate, dextromethorphan hbr
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-8161
Product ID 0067-8161_132b9415-743c-c981-e063-6394a90ae3de
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-06-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00678161
Hyphenated Format 0067-8161

Supplemental Identifiers

RxCUI
247324 1098496 2604579

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 flu relief maximum strength daytime nighttime combo pack (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr and acetaminophen, chlorpheniramine maleate, dextromethorphan hbr (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 15 mg
  • 2 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0067-8161-01) * 20 TABLET in 1 BLISTER PACK (0067-8162-01) * 20 TABLET in 1 BLISTER PACK (0067-8163-01)
source: ndc

Packages (1)

0067-8161-01 1 KIT in 1 CARTON (0067-8161-01) * 20 TABLET in 1 BLISTER PACK (0067-8162-01) * 20 TABLET in 1 BLISTER PACK (0067-8163-01)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Theraflu Flu Relief Maximum Strength Daytime Nighttime Combo Pack ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "132b9415-743c-c981-e063-6394a90ae3de", "openfda": {"rxcui": ["247324", "1098496", "2604579"], "spl_set_id": ["68d3e88a-d1be-410b-92a1-863903b3aa61"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0067-8161-01)  *  20 TABLET in 1 BLISTER PACK (0067-8162-01)  *  20 TABLET in 1 BLISTER PACK (0067-8163-01)", "package_ndc": "0067-8161-01", "marketing_start_date": "20220627"}], "brand_name": "Theraflu Flu Relief Maximum Strength Daytime Nighttime Combo Pack", "product_id": "0067-8161_132b9415-743c-c981-e063-6394a90ae3de", "dosage_form": "KIT", "product_ndc": "0067-8161", "generic_name": "Acetaminophen, Dextromethorphan HBr and Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Flu Relief Maximum Strength", "brand_name_suffix": "Daytime Nighttime Combo Pack", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}