mucinex fast-max dm max and mucinex nighttime cold and flu

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

Identifiers & Regulatory

Product NDC 72854-165
Product ID 72854-165_3ba2cc08-acae-79a8-e063-6394a90af17f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854165
Hyphenated Format 72854-165

Supplemental Identifiers

RxCUI
1020138 2173667 2287760
UPC
0363824014777

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 dm max and mucinex nighttime cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, and 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 (72854-165-26) * 180 mL in 1 BOTTLE (63824-503-66) * 180 mL in 1 BOTTLE (63824-019-66)
source: ndc

Packages (1)

72854-165-26 1 KIT in 1 CARTON (72854-165-26) * 180 mL in 1 BOTTLE (63824-503-66) * 180 mL in 1 BOTTLE (63824-019-66)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Mucinex Fast-Max DM Max and Mucinex Nighttime Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "3ba2cc08-acae-79a8-e063-6394a90af17f", "openfda": {"upc": ["0363824014777"], "rxcui": ["1020138", "2173667", "2287760"], "spl_set_id": ["3ba2cc08-acad-79a8-e063-6394a90af17f"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-165-26)  *  180 mL in 1 BOTTLE (63824-503-66)  *  180 mL in 1 BOTTLE (63824-019-66)", "package_ndc": "72854-165-26", "marketing_start_date": "20250601"}], "brand_name": "Mucinex Fast-Max DM Max and Mucinex Nighttime Cold and Flu", "product_id": "72854-165_3ba2cc08-acae-79a8-e063-6394a90af17f", "dosage_form": "KIT", "product_ndc": "72854-165", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Fast-Max DM Max and Mucinex Nighttime Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}