Package 11822-5160-9
Brand: severe sinus congestion relief maximum strength
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage Facts
Identity
Package NDC
11822-5160-9
Digits Only
1182251609
Product NDC
11822-5160
Description
2 BLISTER PACK in 1 CARTON (11822-5160-9) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
severe sinus congestion relief 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": "19d785fb-e0e3-4834-8b4f-78d4e3a7947f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0011822555708"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["51175d3e-e1c3-4e4d-ad32-61600e87568c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11822-5160-9) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11822-5160-9", "marketing_start_date": "20130630"}], "brand_name": "severe sinus congestion relief Maximum Strength", "product_id": "11822-5160_19d785fb-e0e3-4834-8b4f-78d4e3a7947f", "dosage_form": "TABLET, FILM 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": "11822-5160", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "severe sinus congestion relief", "brand_name_suffix": "Maximum Strength", "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": "20130630", "listing_expiration_date": "20261231"}