Package 63868-071-24
Brand: severe sinus congestion and pain
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
63868-071-24
Digits Only
6386807124
Product NDC
63868-071
Description
2 BLISTER PACK in 1 CARTON (63868-071-24) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
severe sinus congestion and pain
Generic
acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24359114-3c39-dcb1-e063-6394a90a9d99", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515959903"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["1b4e87f8-3f9e-4865-9128-527d2d621593"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63868-071-24) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63868-071-24", "marketing_end_date": "20261231", "marketing_start_date": "20091113"}], "brand_name": "Severe Sinus Congestion and Pain", "product_id": "63868-071_24359114-3c39-dcb1-e063-6394a90a9d99", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "63868-071", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Sinus Congestion and Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20091113"}