Package 79481-7250-8
Brand: sinus severe non drowsy, daytime
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage Facts
Identity
Package NDC
79481-7250-8
Digits Only
7948172508
Product NDC
79481-7250
Description
2 BLISTER PACK in 1 CARTON (79481-7250-8) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sinus severe non drowsy, 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": "6406edfe-8b49-4356-a556-2433d1aebd9f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0713733971928"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["84c30ec9-a7b5-4d2f-95b2-d6fb895945de"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer Distribution, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (79481-7250-8) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "79481-7250-8", "marketing_start_date": "20240611"}], "brand_name": "Sinus Severe Non Drowsy, Daytime", "product_id": "79481-7250_6406edfe-8b49-4356-a556-2433d1aebd9f", "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": "79481-7250", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Meijer Distribution, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Severe", "brand_name_suffix": "Non Drowsy, 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_start_date": "20240611", "listing_expiration_date": "20261231"}