mucinex rapid clear daytime pain, headache, and cough

Generic: acetaminophen, dextromethorphan hydrobromide

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

Drug Facts

Product Profile

Brand Name mucinex rapid clear daytime pain, headache, and cough
Generic Name acetaminophen, dextromethorphan hydrobromide
Labeler rb health (us) llc
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1

Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-214
Product ID 72854-214_37de537d-af42-30fe-e063-6294a90aeb63
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-06-01

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 72854214
Hyphenated Format 72854-214

Supplemental Identifiers

RxCUI
1867684
UPC
0363824999456
UNII
362O9ITL9D 9D2RTI9KYH

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 rapid clear daytime pain, headache, and cough (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (72854-214-16) / 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

72854-214-16 1 BLISTER PACK in 1 CARTON (72854-214-16) / 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (2)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1)

Linked Drug Pages (1)

Mucinex Rapid Clear Daytime Pain, Headache, and Cough ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37de537d-af42-30fe-e063-6294a90aeb63", "openfda": {"upc": ["0363824999456"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["1867684"], "spl_set_id": ["37de53a7-5546-3804-e063-6294a90a0fb5"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (72854-214-16)  / 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "72854-214-16", "marketing_start_date": "20250601"}], "brand_name": "Mucinex Rapid Clear Daytime Pain, Headache, and Cough", "product_id": "72854-214_37de537d-af42-30fe-e063-6294a90aeb63", "dosage_form": "CAPSULE, LIQUID FILLED", "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": "72854-214", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Rapid Clear Daytime Pain, Headache, and Cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}