mucinex fast-max nighttime cold and flu

Generic: acetaminophen, dextromethorphan hydrobromide, 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 nighttime cold and flu
Generic Name acetaminophen, dextromethorphan hydrobromide, triprolidine hydrochloride
Labeler rb health (us) llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/20mL, dextromethorphan hydrobromide 20 mg/20mL, triprolidine hydrochloride 2.5 mg/20mL

Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-143
Product ID 72854-143_3a24c129-074c-c363-e063-6394a90a3a3a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-04-02

Pharmacologic Class

Classes
sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854143
Hyphenated Format 72854-143

Supplemental Identifiers

RxCUI
2173667
UPC
0363824014708
UNII
362O9ITL9D 9D2RTI9KYH YAN7R5L890

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 nighttime cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/20mL
  • 20 mg/20mL
  • 2.5 mg/20mL
source: ndc
Packaging
  • 180 mL in 1 BOTTLE (72854-143-66)
source: ndc

Packages (1)

Ingredients (3)

acetaminophen (650 mg/20mL) dextromethorphan hydrobromide (20 mg/20mL) triprolidine hydrochloride (2.5 mg/20mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a24c129-074c-c363-e063-6394a90a3a3a", "openfda": {"upc": ["0363824014708"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "YAN7R5L890"], "rxcui": ["2173667"], "spl_set_id": ["3a24b06c-00a6-c2ef-e063-6294a90a4d72"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE (72854-143-66)", "package_ndc": "72854-143-66", "marketing_start_date": "20250402"}], "brand_name": "MUCINEX FAST-MAX NIGHTTIME COLD AND FLU", "product_id": "72854-143_3a24c129-074c-c363-e063-6394a90a3a3a", "dosage_form": "SOLUTION", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "72854-143", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCINEX FAST-MAX NIGHTTIME COLD AND FLU", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250402", "listing_expiration_date": "20261231"}