Package 70000-0080-1

Brand: sinus relief severe congestion and pain

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70000-0080-1
Digits Only 7000000801
Product NDC 70000-0080
Description

2 BLISTER PACK in 1 CARTON (70000-0080-1) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2028-02-28
Brand sinus relief severe congestion and pain
Generic acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45ada5e4-1b7f-c75b-e063-6394a90ae3d4", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["645f8075-e33f-4e1a-9249-7368261cdcb9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CARDINAL HEALTH"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (70000-0080-1)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "70000-0080-1", "marketing_end_date": "20280228", "marketing_start_date": "20210127"}], "brand_name": "Sinus Relief Severe Congestion and Pain", "product_id": "70000-0080_45ada5e4-1b7f-c75b-e063-6394a90ae3d4", "dosage_form": "TABLET, 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": "70000-0080", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CARDINAL HEALTH", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Relief Severe 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_end_date": "20280228", "marketing_start_date": "20210127"}