NDC 50227-3271 60-second Fluoride Orange Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PURPLE (C48327)
PINK (C48328)
ORANGE (C48331)
GRAPE (C73391)
BUBBLE GUM (C73368)
STRAWBERRY (C73417)
ORANGE (C73406 - ORANGE CREAM)
Code Structure Chart
Product Details
What is NDC 50227-3271?
What are the uses for 60-second Fluoride Orange Cream?
Which are 60-second Fluoride Orange Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are 60-second Fluoride Orange Cream 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:
- WATER (UNII: 059QF0KO0R)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- XANTHAN GUM (UNII: TTV12P4NEE)
- XYLITOL (UNII: VCQ006KQ1E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for 60-second Fluoride Orange Cream?
- RxCUI: 245593 - sodium fluoride 2 % Dental Gel
- RxCUI: 245593 - sodium fluoride 0.02 MG/MG Oral Gel
- RxCUI: 245593 - sodium fluoride 2 % (fluoride ion 1.23 % ) Dental Gel
- RxCUI: 245593 - sodium fluoride 2.09 % (fluoride ion 1.23 % ) Dental Gel
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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".