NDC 54868-5337 Fluticasone Propionate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5337 - Fluticasone Propionate
Product Packages
NDC Code 54868-5337-0
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
NDC Code 54868-5337-1
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 54868-5337?
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:
- CETETH-20 (UNII: I835H2IHHX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- IMIDUREA (UNII: M629807ATL)
What is the NDC to RxNorm Crosswalk for Fluticasone Propionate?
- RxCUI: 895987 - fluticasone propionate 0.05 % Topical Cream
- RxCUI: 895987 - fluticasone propionate 0.5 MG/ML Topical Cream
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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".