Package 59779-275-08
Brand: severe sinus pain and congestion daytime
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage 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
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"}