Package 41250-275-02
Brand: cold relief severe head congestion
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
41250-275-02
Digits Only
4125027502
Product NDC
41250-275
Description
2 BLISTER PACK in 1 CARTON (41250-275-02) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
cold relief severe head congestion
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": "2434d10b-b229-1732-e063-6294a90a8b99", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["cb5e6dd3-5985-4559-b7f9-ce06d5f9b114"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (41250-275-02) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "41250-275-02", "marketing_end_date": "20260930", "marketing_start_date": "20141107"}], "brand_name": "COLD RELIEF SEVERE HEAD CONGESTION", "product_id": "41250-275_2434d10b-b229-1732-e063-6294a90a8b99", "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": "41250-275", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Meijer", "product_type": "HUMAN OTC DRUG", "brand_name_base": "COLD RELIEF SEVERE HEAD CONGESTION", "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_end_date": "20260930", "marketing_start_date": "20141107"}