Package 83324-112-24

Brand: head congestion plus mucus pe

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83324-112-24
Digits Only 8332411224
Product NDC 83324-112
Description

2 BLISTER PACK in 1 CARTON (83324-112-24) / 12 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-08-06
Brand head congestion plus mucus pe
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": "1f195275-59ce-074d-e063-6294a90a5f6d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["990f3232-bc75-45cf-8a50-cd7861d83f98"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (83324-112-24)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "83324-112-24", "marketing_start_date": "20240806"}], "brand_name": "Head Congestion plus Mucus PE", "product_id": "83324-112_1f195275-59ce-074d-e063-6294a90a5f6d", "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": "83324-112", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Head Congestion plus Mucus PE", "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": "20240806", "listing_expiration_date": "20261231"}