NDC 50090-2484 Fluticasone Propionate
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 50090-2484?
What are the uses for Fluticasone Propionate?
Which are Fluticasone Propionate UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W)
- FLUTICASONE (UNII: CUT2W21N7U) (Active Moiety)
Which are Fluticasone Propionate Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Fluticasone Propionate?
- RxCUI: 1797907 - fluticasone propionate 50 MCG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797907 - fluticasone propionate 0.05 MG/ACTUAT Metered Dose Nasal Spray
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Patient Education
Fluticasone Nasal Spray
Nonprescription (over the counter) fluticasone nasal spray is used to relieve symptoms of rhinitis such as sneezing and a runny, stuffy, or itchy nose and itchy, watery eyes caused by hay fever or other allergies (caused by an allergy to pollen, mold, dust, or pets). Prescription fluticasone nasal spray is used to relieve symptoms of nonallergic rhinitis such as sneezing and runny or stuffy nose which are not caused by allergies. Prescription fluticasone nasal spray (Xhance) is used to treat nasal polyps (swelling of the lining of the nose). Fluticasone nasal spray should not be used to treat symptoms (e.g., sneezing, stuffy, runny, itchy nose) caused by the common cold. Fluticasone is in a class of medications called corticosteroids. It works by blocking the release of certain natural substances that cause allergy symptoms.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".