mucinex sinus-max severe congestion and pain
Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex sinus-max severe congestion and pain
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
63824-692
Product ID
63824-692_29a73c17-c071-3284-e063-6394a90aa812
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2017-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63824692
Hyphenated Format
63824-692
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 (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 (63824-692-16) / 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": "29a73c17-c071-3284-e063-6394a90aa812", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["1e243dbe-138f-4346-ba22-ceea01e97052"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63824-692-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "63824-692-16", "marketing_start_date": "20170701"}], "brand_name": "Mucinex Sinus-Max Severe Congestion and Pain", "product_id": "63824-692_29a73c17-c071-3284-e063-6394a90aa812", "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": "63824-692", "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", "brand_name_suffix": "Severe Congestion and Pain", "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": "20170701", "listing_expiration_date": "20261231"}