actinel
Generic: dextromethorphan hbr,guaifenesin,pseudoephedrine hcl
Labeler: actipharma, llcDrug Facts
Product Profile
Brand Name
actinel
Generic Name
dextromethorphan hbr,guaifenesin,pseudoephedrine hcl
Labeler
actipharma, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 15 mg/5mL, guaifenesin 200 mg/5mL, pseudoephedrine hydrochloride 30 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
63102-101
Product ID
63102-101_11f69bba-6b7f-4876-a8ba-123264408164
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2014-09-24
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63102101
Hyphenated Format
63102-101
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
actinel (source: ndc)
Generic Name
dextromethorphan hbr,guaifenesin,pseudoephedrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/5mL
- 200 mg/5mL
- 30 mg/5mL
Packaging
- 474 mL in 1 BOTTLE (63102-101-16)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "11f69bba-6b7f-4876-a8ba-123264408164", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1098227"], "spl_set_id": ["db0cb6ae-0a4d-4232-805a-f3f3a058261f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["ACTIPHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "474 mL in 1 BOTTLE (63102-101-16)", "package_ndc": "63102-101-16", "marketing_start_date": "20140924"}], "brand_name": "ACTINEL", "product_id": "63102-101_11f69bba-6b7f-4876-a8ba-123264408164", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic alpha-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-Adrenergic Agonist [EPC]"], "product_ndc": "63102-101", "generic_name": "Dextromethorphan HBr,Guaifenesin,Pseudoephedrine HCl", "labeler_name": "ACTIPHARMA, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACTINEL", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/5mL"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140924", "listing_expiration_date": "20261231"}