Package 53943-175-02

Brand: cold plus head congestion severe

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53943-175-02
Digits Only 5394317502
Product NDC 53943-175
Description

2 BLISTER PACK in 1 CARTON (53943-175-02) / 12 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-05-16
Brand cold plus head congestion severe
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": "24ade395-a0b3-fcd8-e063-6294a90a7ad0", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0093351015762"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["3430c7e4-e142-407e-bed5-358dd6bd10f7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["DISCOUNT DRUG MART"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (53943-175-02)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "53943-175-02", "marketing_start_date": "20140516"}], "brand_name": "COLD PLUS HEAD CONGESTION SEVERE", "product_id": "53943-175_24ade395-a0b3-fcd8-e063-6294a90a7ad0", "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": "53943-175", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "DISCOUNT DRUG MART", "product_type": "HUMAN OTC DRUG", "brand_name_base": "COLD PLUS HEAD CONGESTION 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": "20140516", "listing_expiration_date": "20261231"}