Package 63868-081-24
Brand: severe cold head congestion
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
63868-081-24
Digits Only
6386808124
Product NDC
63868-081
Description
2 BLISTER PACK in 1 CARTON (63868-081-24) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
severe cold head congestion
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": "2435ad4f-59a9-f2ac-e063-6394a90ae811", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515993358"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["5baa6aab-3959-42ad-b448-a524de81762b"], "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 (63868-081-24) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63868-081-24", "marketing_end_date": "20260930", "marketing_start_date": "20150930"}], "brand_name": "Severe Cold Head Congestion", "product_id": "63868-081_2435ad4f-59a9-f2ac-e063-6394a90ae811", "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": "63868-081", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Cold Head Congestion", "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": "20260930", "marketing_start_date": "20150930"}