Package 30142-727-08

Brand: sinus congestion and pain

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 30142-727-08
Digits Only 3014272708
Product NDC 30142-727
Description

2 BLISTER PACK in 1 CARTON (30142-727-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-05-31
Brand sinus congestion and pain
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": "d20ae731-15e0-46a9-bf5f-72f6c9c0c337", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041260003493"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["6aaed3fe-ce35-4533-aea4-80096ce8e57a"], "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 (30142-727-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "30142-727-08", "marketing_start_date": "20190531"}], "brand_name": "Sinus Congestion and Pain", "product_id": "30142-727_d20ae731-15e0-46a9-bf5f-72f6c9c0c337", "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": "30142-727", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Congestion and Pain", "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": "20190531", "listing_expiration_date": "20261231"}