Package 30142-732-08

{"route": ["ORAL"], "spl_id": "6b947986-ddfd-4324-9638-053320f55456", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041260003493"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["1022767d-a456-4fbc-95cf-91337c74c330"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (30142-732-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "30142-732-08", "marketing_start_date": "20251024"}], "brand_name": "Daytime Sinus Severe", "product_id": "30142-732_6b947986-ddfd-4324-9638-053320f55456", "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": "30142-732", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Sinus", "brand_name_suffix": "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_start_date": "20251024", "listing_expiration_date": "20261231"}