Package 63868-722-20

Brand: mucus relief sinus severe congestion relief

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63868-722-20
Digits Only 6386872220
Product NDC 63868-722
Description

2 BLISTER PACK in 1 CARTON (63868-722-20) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-06-10
Brand mucus relief sinus severe congestion relief
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": "284bee95-f715-99d1-e063-6394a90a62a8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515994072"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["0ea270b7-9c28-49fb-9615-c4afdbdbc8f1"], "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 (63868-722-20)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63868-722-20", "marketing_start_date": "20150610"}], "brand_name": "Mucus Relief Sinus Severe Congestion Relief", "product_id": "63868-722_284bee95-f715-99d1-e063-6394a90a62a8", "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": "63868-722", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Sinus Severe Congestion Relief", "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": "20150610", "listing_expiration_date": "20261231"}