Package 63868-103-24
Brand: head congestion mucus pe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
63868-103-24
Digits Only
6386810324
Product NDC
63868-103
Description
2 BLISTER PACK in 1 CARTON (63868-103-24) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
head congestion mucus pe
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": "284c2e2c-017d-cc45-e063-6394a90a8d6a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515987395"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["0955d856-cc4e-4ef2-8bc0-1a632a5b5f79"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63868-103-24) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63868-103-24", "marketing_start_date": "20220803"}], "brand_name": "Head Congestion Mucus PE", "product_id": "63868-103_284c2e2c-017d-cc45-e063-6394a90a8d6a", "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": "63868-103", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Head Congestion Mucus PE", "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_start_date": "20220803", "listing_expiration_date": "20261231"}