Package 69842-651-01

Brand: congestion and headache

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 69842-651-01
Digits Only 6984265101
Product NDC 69842-651
Description

3 BLISTER PACK in 1 CARTON (69842-651-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2020-10-14
Brand congestion and headache
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": "4cf2f7cf-aedd-412a-b2af-9b00edf8ff73", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050428285107"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["432c3ec4-7595-4213-94e3-ce41af91804e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (69842-651-01)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "69842-651-01", "marketing_start_date": "20201014"}], "brand_name": "Congestion and Headache", "product_id": "69842-651_4cf2f7cf-aedd-412a-b2af-9b00edf8ff73", "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": "69842-651", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Congestion and Headache", "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_start_date": "20130630", "listing_expiration_date": "20261231"}