mucinex childrens cough and congestion
Generic: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex childrens cough and congestion
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler
rb health (us) llc
Dosage Form
SUSPENSION
Routes
Active Ingredients
dextromethorphan hydrobromide 5 mg/5mL, guaifenesin 100 mg/5mL, phenylephrine hydrochloride 2.5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
63824-947
Product ID
63824-947_29a67ae8-e460-57aa-e063-6394a90afeb5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2018-03-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63824947
Hyphenated Format
63824-947
Supplemental Identifiers
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 and congestion (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
- 100 mg/5mL
- 2.5 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (63824-947-11) / 201 mL in 1 BOTTLE
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29a67ae8-e460-57aa-e063-6394a90afeb5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "spl_set_id": ["d9e5a8d7-814c-4ab1-bb05-e4cb9155978e"], "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 (63824-947-11) / 201 mL in 1 BOTTLE", "package_ndc": "63824-947-11", "marketing_start_date": "20180330"}], "brand_name": "Mucinex Childrens Cough and Congestion", "product_id": "63824-947_29a67ae8-e460-57aa-e063-6394a90afeb5", "dosage_form": "SUSPENSION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "63824-947", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Childrens Cough and Congestion", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "2.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180330", "listing_expiration_date": "20261231"}