tussin multi symptom cold cf adult
Generic: dextromethorphan hbr, guaifenesin, phenylephrine
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
tussin multi symptom cold cf adult
Generic Name
dextromethorphan hbr, guaifenesin, phenylephrine
Labeler
major pharmaceuticals
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 200 mg/10mL, phenylephrine hydrochloride 10 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6537
Product ID
0904-6537_7bcf4ed4-fdc2-4408-bc9b-ebbdae3aee70
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2015-11-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046537
Hyphenated Format
0904-6537
Supplemental Identifiers
RxCUI
UPC
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
tussin multi symptom cold cf adult (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin, phenylephrine (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/10mL
- 200 mg/10mL
- 10 mg/10mL
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (0904-6537-20) / 118 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7bcf4ed4-fdc2-4408-bc9b-ebbdae3aee70", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0309046537205"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1044949"], "spl_set_id": ["a9958b7d-7060-422b-a098-c1925c246081"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (0904-6537-20) / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0904-6537-20", "marketing_start_date": "20151130"}], "brand_name": "Tussin Multi Symptom Cold CF Adult", "product_id": "0904-6537_7bcf4ed4-fdc2-4408-bc9b-ebbdae3aee70", "dosage_form": "LIQUID", "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": "0904-6537", "generic_name": "Dextromethorphan HBr, Guaifenesin, Phenylephrine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tussin Multi Symptom Cold CF", "brand_name_suffix": "Adult", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/10mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/10mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/10mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20151130", "listing_expiration_date": "20261231"}