Package 68016-504-24

Brand: sinus severe

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package 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
Discontinued 2026-07-31
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"}