Package 68016-504-24
Brand: sinus severe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
68016-504-24
Digits Only
6801650424
Product NDC
68016-504
Description
2 BLISTER PACK in 1 CARTON (68016-504-24) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sinus 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": "2433dde9-0eed-313a-e063-6294a90a9441", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986024962"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["01a1183d-deec-40ca-94da-a6e40b7af2c7"], "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 (68016-504-24) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "68016-504-24", "marketing_end_date": "20260731", "marketing_start_date": "20091101"}], "brand_name": "Sinus Severe", "product_id": "68016-504_2433dde9-0eed-313a-e063-6294a90a9441", "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": "68016-504", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus 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": "20091101"}