NDC 65954-385 Colgate Optic White Beauty Radiant
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Product Details
What is NDC 65954-385?
What are the uses for Colgate Optic White Beauty Radiant?
Which are Colgate Optic White Beauty Radiant UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Colgate Optic White Beauty Radiant 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)
- POVIDONE K15 (UNII: E54VE15114)
- PEG/PPG-116/66 COPOLYMER (UNII: JP0CK963E0)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
What is the NDC to RxNorm Crosswalk for Colgate Optic White Beauty Radiant?
- RxCUI: 1038995 - sodium monofluorophosphate 1.14 % Toothpaste
- RxCUI: 1038995 - sodium monofluorophosphate 0.0114 MG/MG Toothpaste
- RxCUI: 1038995 - sodium monofluorophosphate 1.14 % (fluoride ion 0.17 % )Toothpaste
- RxCUI: 1038995 - sodium monofluorophosphate 1.14 % (fluoride ion 0.19 % )Toothpaste
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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".