NDC 72805-160 Luster Premium White Pro Sonic Dental Whitening System
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72805 - French Transit, Ltd.
- 72805-160 - Luster Premium White
Product Packages
NDC Code 72805-160-13
Package Description: 1 KIT in 1 CARTON * 177 mL in 1 TUBE * 7 mL in 1 TUBE * 28 g in 1 TUBE (72805-150-28)
Product Details
What is NDC 72805-160?
What are the uses for Luster Premium White Pro Sonic Dental Whitening System?
Which are Luster Premium White Pro Sonic Dental Whitening System 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 Premium White Pro Sonic Dental Whitening System 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 PYROPHOSPHATE (UNII: X69NU20D19)
- STARCH, CORN (UNII: O8232NY3SJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
What is the NDC to RxNorm Crosswalk for Luster Premium White Pro Sonic Dental Whitening System?
- 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".