Package 70000-0141-1

Brand: mucus relief pe sinus congestion

Generic: guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 70000-0141-1
Digits Only 7000001411
Product NDC 70000-0141
Description

1 BOTTLE, PLASTIC in 1 CARTON (70000-0141-1) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2006-04-15
Brand mucus relief pe sinus congestion
Generic guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "59fa21ab-5e68-467b-90bf-2c8a3e96709b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295143584"], "unii": ["495W7451VQ", "04JA59TNSJ"], "rxcui": ["1304111"], "spl_set_id": ["b9129c7b-c869-436f-ab95-269610ef2d9f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70000-0141-1)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "70000-0141-1", "marketing_start_date": "20060415"}], "brand_name": "Mucus Relief PE Sinus Congestion", "product_id": "70000-0141_59fa21ab-5e68-467b-90bf-2c8a3e96709b", "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": "70000-0141", "generic_name": "Guaifenesin, Phenylephrine HCl", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief PE Sinus Congestion", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20060415", "listing_expiration_date": "20261231"}