Package 59779-275-08

Brand: severe sinus pain and congestion daytime

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 59779-275-08
Digits Only 5977927508
Product NDC 59779-275
Description

2 BLISTER PACK in 1 CARTON (59779-275-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2028-04-30
Brand severe sinus pain and congestion daytime
Generic acetaminophen, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8505a29b-8fe3-49eb-870c-f076b4c4826f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050428348505"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["4af347ce-9745-4a5e-8ce9-e7c97a0a6cc7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (59779-275-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "59779-275-08", "marketing_end_date": "20280430", "marketing_start_date": "20050806"}], "brand_name": "Severe Sinus Pain and Congestion Daytime", "product_id": "59779-275_8505a29b-8fe3-49eb-870c-f076b4c4826f", "dosage_form": "TABLET, FILM 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": "59779-275", "generic_name": "acetaminophen, guaifenesin, phenylephrine HCl", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Sinus Pain and Congestion", "brand_name_suffix": "Daytime", "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": "20280430", "marketing_start_date": "20050806"}