mucinex fast-max day cold and flu and night cold and flu maximum strength

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, and phenylephrine hydrochloride

Labeler: rb health (us) llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucinex fast-max day cold and flu and night cold and flu maximum strength
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, and phenylephrine hydrochloride
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-144
Product ID 72854-144_29f6bf23-ec52-1b42-e063-6394a90a3a47
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-06-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854144
Hyphenated Format 72854-144

Supplemental Identifiers

RxCUI
1297288 1656815 2634364

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 mucinex fast-max day cold and flu and night cold and flu maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (72854-144-10) * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

72854-144-10 1 KIT in 1 CARTON (72854-144-10) * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Mucinex Fast-Max Day Cold and Flu and Night Cold and Flu Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "29f6bf23-ec52-1b42-e063-6394a90a3a47", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["fe44d1ee-1e03-b74f-e053-6294a90a8bb4"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-144-10)  *  4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "72854-144-10", "marketing_start_date": "20230614"}], "brand_name": "Mucinex Fast-Max Day Cold and Flu and Night Cold and Flu Maximum Strength", "product_id": "72854-144_29f6bf23-ec52-1b42-e063-6394a90a3a47", "dosage_form": "KIT", "product_ndc": "72854-144", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, and Phenylephrine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Fast-Max Day Cold and Flu and Night Cold and Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230614", "listing_expiration_date": "20261231"}