Package 63868-722-20
Brand: mucus relief sinus severe congestion relief
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage 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
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"}