tukol multi symptom cold
Generic: dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler: genomma lab usa, inc.Drug Facts
Product Profile
Brand Name
tukol multi symptom cold
Generic Name
dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler
genomma lab usa, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 10 mg/5mL, guaifenesin 100 mg/5mL, phenylephrine hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50066-504
Product ID
50066-504_4c7fab8b-ba17-4210-9f16-05fdac6cf62b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2012-05-15
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50066504
Hyphenated Format
50066-504
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
tukol multi symptom cold (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
- 100 mg/5mL
- 5 mg/5mL
Packaging
- 118 mL in 1 BOTTLE (50066-504-24)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c7fab8b-ba17-4210-9f16-05fdac6cf62b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1044949"], "spl_set_id": ["aef2ad43-145d-4abc-bccc-2c5fdd6882f9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Genomma Lab USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (50066-504-24)", "package_ndc": "50066-504-24", "marketing_start_date": "20120515"}], "brand_name": "Tukol Multi Symptom Cold", "product_id": "50066-504_4c7fab8b-ba17-4210-9f16-05fdac6cf62b", "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": "50066-504", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Genomma Lab USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tukol Multi Symptom Cold", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120515", "listing_expiration_date": "20261231"}