Package 0363-6028-09

Brand: sinus pressure and pain

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0363-6028-09
Digits Only 0363602809
Product NDC 0363-6028
Description

2 BLISTER PACK in 1 CARTON (0363-6028-09) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-12-31
Brand sinus pressure 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": "da9726d3-762b-4e24-8d5f-091d21e07e4d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917168609"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["c378acaf-389a-4afb-a4f0-e367a907a468"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0363-6028-09)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0363-6028-09", "marketing_end_date": "20271231", "marketing_start_date": "20130503"}], "brand_name": "Sinus Pressure and Pain", "product_id": "0363-6028_da9726d3-762b-4e24-8d5f-091d21e07e4d", "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": "0363-6028", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Pressure 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_end_date": "20271231", "marketing_start_date": "20130503"}