Package 42507-375-02
Brand: cold plus head congestion severe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
42507-375-02
Digits Only
4250737502
Product NDC
42507-375
Description
2 BLISTER PACK in 1 CARTON (42507-375-02) / 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": "42b526b1-f846-84c6-e063-6394a90aef17", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0075450842647"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["409540c0-1bab-9969-e063-6394a90a47c1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["HYVEE INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (42507-375-02) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "42507-375-02", "marketing_start_date": "20251103"}], "brand_name": "Cold plus Head Congestion Severe", "product_id": "42507-375_42b526b1-f846-84c6-e063-6394a90aef17", "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": "42507-375", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "HYVEE INC", "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": "20251103", "listing_expiration_date": "20261231"}