tussin multi symptom cold cf adult

Generic: dextromethorphan hbr, guaifenesin, phenylephrine

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tussin multi symptom cold cf adult
Generic Name dextromethorphan hbr, guaifenesin, phenylephrine
Labeler major pharmaceuticals
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 200 mg/10mL, phenylephrine hydrochloride 10 mg/10mL

Manufacturer
Major Pharmaceuticals

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)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046537
Hyphenated Format 0904-6537

Supplemental Identifiers

RxCUI
1044949
UPC
0309046537205
UNII
9D2RTI9KYH 495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/10mL
  • 200 mg/10mL
  • 10 mg/10mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (0904-6537-20) / 118 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (3)

dextromethorphan hydrobromide (20 mg/10mL) guaifenesin (200 mg/10mL) phenylephrine hydrochloride (10 mg/10mL)

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"}