mucinex fast-max kickstart severe congestion and cough and mucinex fast-max nighttime cold and flu

Generic: dextromethorphan hydrobromide, guaifenesin, acetaminophen,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 kickstart severe congestion and cough and mucinex fast-max nighttime cold and flu
Generic Name dextromethorphan hydrobromide, guaifenesin, acetaminophen,triprolidine hydrochloride
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-160
Product ID 72854-160_34fd2458-9ace-cdf7-e063-6394a90a3d0a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-04-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854160
Hyphenated Format 72854-160

Supplemental Identifiers

RxCUI
1020138 2173667 2287760

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 kickstart severe congestion and cough and mucinex fast-max nighttime cold and flu (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin, acetaminophen,triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 20 ml
  • 20 mg
  • 400 mg
  • 650 mg
  • 2.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (72854-160-26) * 180 mL in 1 BOTTLE (72854-143-66) * 180 LIQUID in 1 BOTTLE (72854-159-66)
source: ndc

Packages (1)

72854-160-26 1 KIT in 1 CARTON (72854-160-26) * 180 mL in 1 BOTTLE (72854-143-66) * 180 LIQUID in 1 BOTTLE (72854-159-66)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Mucinex Fast-Max Kickstart Severe Congestion and Cough and Mucinex Fast-Max Nighttime Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "34fd2458-9ace-cdf7-e063-6394a90a3d0a", "openfda": {"rxcui": ["1020138", "2173667", "2287760"], "spl_set_id": ["34fd2458-9acd-cdf7-e063-6394a90a3d0a"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-160-26)  *  180 mL in 1 BOTTLE (72854-143-66)  *  180 LIQUID in 1 BOTTLE (72854-159-66)", "package_ndc": "72854-160-26", "marketing_start_date": "20250402"}], "brand_name": "Mucinex Fast-Max Kickstart Severe Congestion and Cough and Mucinex Fast-Max Nighttime Cold and Flu", "product_id": "72854-160_34fd2458-9ace-cdf7-e063-6394a90a3d0a", "dosage_form": "KIT", "product_ndc": "72854-160", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, Acetaminophen,Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Fast-Max Kickstart Severe Congestion and Cough and Mucinex Fast-Max Nighttime Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250402", "listing_expiration_date": "20261231"}