Package 55910-757-09
Brand: mucus relief congestion and headache maximum strength
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage 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
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"}