mucinex sinus-max severe congestion and pain maximum strength
Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex sinus-max severe congestion and pain maximum strength
Generic Name
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler
rb health (us) llc
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72854-203
Product ID
72854-203_29f6eafd-b7a3-6422-e063-6294a90a6d1b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2021-07-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72854203
Hyphenated Format
72854-203
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 sinus-max severe congestion and pain maximum strength (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (72854-203-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29f6eafd-b7a3-6422-e063-6294a90a6d1b", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["ad4e0e4d-cc1f-4176-835f-3ba76564c634"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72854-203-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "72854-203-16", "marketing_start_date": "20210726"}], "brand_name": "Mucinex Sinus-Max Severe Congestion and Pain Maximum Strength", "product_id": "72854-203_29f6eafd-b7a3-6422-e063-6294a90a6d1b", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "72854-203", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Sinus-Max Severe Congestion and Pain", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210726", "listing_expiration_date": "20261231"}