Package 53943-175-02
Brand: cold plus head congestion severe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage 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
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"}