mucinex fast max liquid cold and flu kickstart and mucinex nightshift kickstart

Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, triprolidine hci

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

Drug Facts

Product Profile

Brand Name mucinex fast max liquid cold and flu kickstart and mucinex nightshift kickstart
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, triprolidine hci
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-139
Product ID 72854-139_29f66987-f057-99e7-e063-6294a90a497c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854139
Hyphenated Format 72854-139

Supplemental Identifiers

RxCUI
1116572 2173662 2637727

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 liquid cold and flu kickstart and mucinex nightshift kickstart (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, triprolidine hci (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 650 mg
  • 20 mg
  • 400 mg
  • 10 mg
  • 2.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (72854-139-26) * 180 mL in 1 BOTTLE (72854-138-66) * 180 mL in 1 BOTTLE (72854-140-66)
source: ndc

Packages (1)

72854-139-26 1 KIT in 1 CARTON (72854-139-26) * 180 mL in 1 BOTTLE (72854-138-66) * 180 mL in 1 BOTTLE (72854-140-66)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

MUCINEX FAST MAX Liquid Cold and Flu Kickstart and MUCINEX Nightshift Kickstart ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "29f66987-f057-99e7-e063-6294a90a497c", "openfda": {"rxcui": ["1116572", "2173662", "2637727"], "spl_set_id": ["fdb70793-5dd1-0455-e053-6394a90ac621"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-139-26)  *  180 mL in 1 BOTTLE (72854-138-66)  *  180 mL in 1 BOTTLE (72854-140-66)", "package_ndc": "72854-139-26", "marketing_start_date": "20230501"}], "brand_name": "MUCINEX FAST MAX Liquid Cold and Flu Kickstart and MUCINEX Nightshift Kickstart", "product_id": "72854-139_29f66987-f057-99e7-e063-6294a90a497c", "dosage_form": "KIT", "product_ndc": "72854-139", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, Triprolidine HCI", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCINEX FAST MAX Liquid Cold and Flu Kickstart and MUCINEX Nightshift Kickstart", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}