Package 68016-717-24
Brand: cold and head congestion severe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
68016-717-24
Digits Only
6801671724
Product NDC
68016-717
Description
2 BLISTER PACK in 1 CARTON (68016-717-24) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
cold and head congestion severe
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": "2434193f-6ba3-923d-e063-6394a90aec0c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986032455"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["f3163a9f-e916-4b61-80ab-ed5f1e7579f8"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68016-717-24) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "68016-717-24", "marketing_end_date": "20260731", "marketing_start_date": "20150601"}], "brand_name": "Cold and Head Congestion Severe", "product_id": "68016-717_2434193f-6ba3-923d-e063-6394a90aec0c", "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": "68016-717", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Head Congestion Severe", "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": "20260731", "marketing_start_date": "20150601"}