Package 70000-0080-1
Brand: sinus relief severe congestion and pain
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage 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
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"}