tusnel dm
Generic: dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler: llorens pharmaceutical international division, inc.Drug Facts
Product Profile
Brand Name
tusnel dm
Generic Name
dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler
llorens pharmaceutical international division, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/5mL, guaifenesin 400 mg/5mL, phenylephrine hydrochloride 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
54859-517
Product ID
54859-517_471f0d89-3e47-8d6d-e063-6294a90a508d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2019-05-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54859517
Hyphenated Format
54859-517
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
tusnel dm (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/5mL
- 400 mg/5mL
- 10 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (54859-517-16)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "471f0d89-3e47-8d6d-e063-6294a90a508d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0354859517166"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1091331"], "spl_set_id": ["fe457e6d-422d-496c-bcb9-33594f3c42ff"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Llorens Pharmaceutical International Division, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (54859-517-16)", "package_ndc": "54859-517-16", "marketing_start_date": "20190501"}], "brand_name": "Tusnel DM", "product_id": "54859-517_471f0d89-3e47-8d6d-e063-6294a90a508d", "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": "54859-517", "generic_name": "Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "Llorens Pharmaceutical International Division, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tusnel", "brand_name_suffix": "DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}