mucinex childrens multi-symptom cold
Generic: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex childrens multi-symptom cold
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
63824-949
Product ID
63824-949_29a6b243-5f52-62c4-e063-6394a90adfb9
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
63824949
Hyphenated Format
63824-949
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 multi-symptom cold (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 (63824-949-01) / 118 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": "29a6b243-5f52-62c4-e063-6394a90adfb9", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "spl_set_id": ["771d7fd8-184f-48a3-90ed-e8f00159d97e"], "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 (63824-949-01) / 118 mL in 1 BOTTLE", "package_ndc": "63824-949-01", "marketing_start_date": "20180330"}], "brand_name": "Mucinex Childrens Multi-Symptom Cold", "product_id": "63824-949_29a6b243-5f52-62c4-e063-6394a90adfb9", "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": "63824-949", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Childrens Multi-Symptom Cold", "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"}