Package 67091-212-24

Brand: cold and head congestion relief severe

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 67091-212-24
Digits Only 6709121224
Product NDC 67091-212
Description

2 BLISTER PACK in 1 CARTON (67091-212-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2005-08-06
Brand cold and head congestion relief severe
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": "2d9c9b1f-1049-497e-9d6e-ab7e8777bf46", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0070552241299"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["a39778ba-1f63-4495-8e9b-44b0bdd7f71a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["WinCo Foods, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (67091-212-24)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67091-212-24", "marketing_start_date": "20050806"}], "brand_name": "Cold and Head Congestion Relief Severe", "product_id": "67091-212_2d9c9b1f-1049-497e-9d6e-ab7e8777bf46", "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": "67091-212", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "WinCo Foods, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Head Congestion Relief", "brand_name_suffix": "Severe", "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": "20050806", "listing_expiration_date": "20261231"}