mucinex nightshift severe cold and flu
Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, and triprolidine hydrochloride
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex nightshift severe cold and flu
Generic Name
acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, and triprolidine hydrochloride
Labeler
rb health (us) llc
Dosage Form
SOLUTION
Routes
Active Ingredients
acetaminophen 650 mg/20mL, dextromethorphan hydrobromide 20 mg/20mL, phenylephrine hydrochloride 10 mg/20mL, triprolidine hydrochloride 2.5 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
63824-504
Product ID
63824-504_29a7479a-730e-b01e-e063-6394a90aeb85
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2020-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63824504
Hyphenated Format
63824-504
Supplemental Identifiers
RxCUI
UPC
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 nightshift severe cold and flu (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, and triprolidine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/20mL
- 20 mg/20mL
- 10 mg/20mL
- 2.5 mg/20mL
Packaging
- 180 mL in 1 BOTTLE (63824-504-66)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29a7479a-730e-b01e-e063-6394a90aeb85", "openfda": {"upc": ["0363824995144"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ", "YAN7R5L890"], "rxcui": ["2173662"], "spl_set_id": ["a14bc0d1-9b05-4a21-aaa8-95d4d073b9ed"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE (63824-504-66)", "package_ndc": "63824-504-66", "marketing_start_date": "20200601"}], "brand_name": "Mucinex Nightshift Severe Cold and Flu", "product_id": "63824-504_29a7479a-730e-b01e-e063-6394a90aeb85", "dosage_form": "SOLUTION", "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": "63824-504", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Nightshift Severe Cold and Flu", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}