NDC 54868-6168 Veramyst
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6168 - Veramyst
Product Characteristics
Product Packages
NDC Code 54868-6168-0
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 120 SPRAY, METERED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-6168?
What are the uses for Veramyst?
Which are Veramyst UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUTICASONE FUROATE (UNII: JS86977WNV)
- FLUTICASONE (UNII: CUT2W21N7U) (Active Moiety)
Which are Veramyst 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)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Veramyst?
- RxCUI: 1797890 - fluticasone furoate 27.5 MCG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797890 - fluticasone furoate 0.0275 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797892 - Veramyst 27.5 MCG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797892 - fluticasone furoate 0.0275 MG/ACTUAT Metered Dose Nasal Spray [Veramyst]
- RxCUI: 1797892 - Veramyst 0.0275 MG/ACTUAT Metered Dose Nasal Spray
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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".