NDC 57353-106 Luster Power White Deep Stain Eraser
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 57353-106?
What are the uses for Luster Power White Deep Stain Eraser?
Which are Luster Power White Deep Stain Eraser 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 Luster Power White Deep Stain Eraser 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)
- STARCH, CORN (UNII: O8232NY3SJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- WATER (UNII: 059QF0KO0R)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- CARBOMER 934 (UNII: Z135WT9208)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- PIROCTONE OLAMINE (UNII: A4V5C6R9FB)
What is the NDC to RxNorm Crosswalk for Luster Power White Deep Stain Eraser?
- RxCUI: 1546238 - sodium monofluorophosphate 0.88 % Toothpaste
- RxCUI: 1546238 - sodium monofluorophosphate 0.0088 MG/MG Toothpaste
- RxCUI: 1546238 - sodium monofluorophosphate 0.88 % (fluoride ion 0.115 % )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".