Package 41250-275-02

Brand: cold relief severe head congestion

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package 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
Discontinued 2026-09-30
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"}