Package 55910-757-09

Brand: mucus relief congestion and headache maximum strength

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 55910-757-09
Digits Only 5591075709
Product NDC 55910-757
Description

266 mL in 1 BOTTLE, PLASTIC (55910-757-09)

Marketing

Marketing Status
Marketed Since 2019-06-01
Brand mucus relief congestion and headache maximum strength
Generic acetaminophen, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c8a19e46-6ec9-40dc-922a-732e1528aadf", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0715256702355"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1116568"], "spl_set_id": ["2638b541-e680-4949-a7c7-fcee165cbc92"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "266 mL in 1 BOTTLE, PLASTIC (55910-757-09)", "package_ndc": "55910-757-09", "marketing_start_date": "20190601"}], "brand_name": "Mucus Relief Congestion and Headache Maximum Strength", "product_id": "55910-757_c8a19e46-6ec9-40dc-922a-732e1528aadf", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55910-757", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCL", "labeler_name": "Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Congestion and Headache", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}