mucinex childrens cough
Generic: dextromethorphan hydrobromide and guaifenesin
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex childrens cough
Generic Name
dextromethorphan hydrobromide and guaifenesin
Labeler
rb health (us) llc
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 5 mg/5mL, guaifenesin 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
63824-946
Product ID
63824-946_369d5bd6-8c4e-5438-e063-6294a90a0481
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2018-05-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63824946
Hyphenated Format
63824-946
Supplemental Identifiers
RxCUI
UNII
NUI
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 childrens cough (source: ndc)
Generic Name
dextromethorphan hydrobromide and guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
- 100 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (63824-946-03) / 118 mL in 1 BOTTLE
- 3 BOTTLE in 1 CARTON (63824-946-34) / 118 mL in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "369d5bd6-8c4e-5438-e063-6294a90a0481", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["b8132c81-5291-431a-ad3a-ec8a3eb21c19"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63824-946-03) / 118 mL in 1 BOTTLE", "package_ndc": "63824-946-03", "marketing_start_date": "20180501"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (63824-946-34) / 118 mL in 1 BOTTLE", "package_ndc": "63824-946-34", "marketing_start_date": "20240725"}], "brand_name": "Mucinex Childrens Cough", "product_id": "63824-946_369d5bd6-8c4e-5438-e063-6294a90a0481", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "63824-946", "generic_name": "Dextromethorphan Hydrobromide and Guaifenesin", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Childrens", "brand_name_suffix": "Cough", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}