NDC 53567-0101 Supersmile Professional Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53567 - Robell Research, Inc.
- 53567-0101 - Supersmile Professional
Product Characteristics
Product Packages
NDC Code 53567-0101-6
Package Description: 227 g in 1 TUBE
Product Details
What is NDC 53567-0101?
What are the uses for Supersmile Professional Whitening?
Which are Supersmile Professional Whitening 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 Supersmile Professional Whitening 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)
- CALCIUM PEROXIDE (UNII: 7FRO2ENO91)
- SODIUM PERBORATE (UNII: Y52BK1W96C)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- STARCH, CORN (UNII: O8232NY3SJ)
- SACCHARIN (UNII: FST467XS7D)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
What is the NDC to RxNorm Crosswalk for Supersmile Professional Whitening?
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )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".