Package 21130-615-09
Brand: severe sinus congestion and pain maximum strength
Generic: acetaminophen, guaifenesin, phenylephrine hclPackage Facts
Identity
Package NDC
21130-615-09
Digits Only
2113061509
Product NDC
21130-615
Description
2 BLISTER PACK in 1 CARTON (21130-615-09) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
severe sinus congestion and pain 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": "84f69757-d93a-4844-9ce7-85498d1ca623", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0321130763857"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["b7b1c3cc-fdf3-4e75-8c3f-2e832f09a887"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (21130-615-09) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "21130-615-09", "marketing_start_date": "20130630"}], "brand_name": "Severe Sinus Congestion and Pain Maximum Strength", "product_id": "21130-615_84f69757-d93a-4844-9ce7-85498d1ca623", "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": "21130-615", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Sinus Congestion and Pain", "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"}