mucinex fast-max day severe congestion and cough and mucinex nightshift night cold and flu maximum strength

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and triprolidine 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 severe congestion and cough and mucinex nightshift night cold and flu maximum strength
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and triprolidine hydrochloride
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-242
Product ID 72854-242_29f6d3f8-4b0f-7350-e063-6394a90afdcf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854242
Hyphenated Format 72854-242

Supplemental Identifiers

RxCUI
1372652 2549034 2560238

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 severe congestion and cough and mucinex nightshift night cold and flu maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 10 mg
  • 200 mg
  • 5 mg
  • 325 mg
  • 1.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (72854-242-40) * 6 TABLET, COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

72854-242-40 1 KIT in 1 CARTON (72854-242-40) * 6 TABLET, COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "29f6d3f8-4b0f-7350-e063-6394a90afdcf", "openfda": {"rxcui": ["1372652", "2549034", "2560238"], "spl_set_id": ["a401eb92-60b6-427d-a677-29371a3150be"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-242-40)  *  6 TABLET, COATED in 1 BLISTER PACK *  4 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-242-40", "marketing_start_date": "20210701"}], "brand_name": "Mucinex Fast-Max Day Severe Congestion and Cough and Mucinex Nightshift Night Cold and Flu Maximum Strength", "product_id": "72854-242_29f6d3f8-4b0f-7350-e063-6394a90afdcf", "dosage_form": "KIT", "product_ndc": "72854-242", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Fast-Max Day Severe Congestion and Cough and Mucinex Nightshift Night Cold and Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}