Package 0363-6028-09
Brand: sinus pressure and pain
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage 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
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"}