NDC 52261-0204 Fiore Rx Pixie Dust Pink Antifungal Nail Polish
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 52261-0204?
What are the uses for Fiore Rx Pixie Dust Pink Antifungal Nail Polish?
Which are Fiore Rx Pixie Dust Pink Antifungal Nail Polish UNII Codes?
The UNII codes for the active ingredients in this product are:
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- UNDECYLENIC ACID (UNII: K3D86KJ24N) (Active Moiety)
Which are Fiore Rx Pixie Dust Pink Antifungal Nail Polish 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:
- BUTYL ACETATE (UNII: 464P5N1905)
- ETHYL ACETATE (UNII: 76845O8NMZ)
- PYROXYLIN (UNII: KYR8BR2X6O)
- POLYESTER-10 (UNII: 212N9O2MMZ)
- ACETYLTRIBUTYL CITRATE (UNII: 0ZBX0N59RZ)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH)
- BENTOQUATAM (UNII: 7F465U79Q1)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BENZORESORCINOL (UNII: LJ54R4Z029)
- MICA (UNII: V8A1AW0880)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- TRIMETHYLPENTANEDIYL DIBENZOATE (UNII: Y8PB83G67A)
- D&C RED NO. 34 (UNII: BAN556989E)
- D&C RED NO. 6 (UNII: 481744AI4O)
- STANNIC OXIDE (UNII: KM7N50LOS6)
What is the NDC to RxNorm Crosswalk for Fiore Rx Pixie Dust Pink Antifungal Nail Polish?
- RxCUI: 1437977 - Undecylenic Acid 3 % Topical Solution
- RxCUI: 1437977 - undecylenic acid 30 MG/ML Topical Solution
- RxCUI: 1437982 - Fiore Rx Antifungal 3 % Nail Polish
- RxCUI: 1437982 - undecylenic acid 30 MG/ML Topical Solution [Fiore]
- RxCUI: 1437982 - Fiore 30 MG/ML Topical Solution
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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".