NDC 70635-0003 Lutooth Tooth Whitening Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70635 - Quorum Bio Co.,ltd
- 70635-0003 - Lutooth Tooth Whitening Kit
Product Packages
NDC Code 70635-0003-4
Package Description: 2 APPLICATOR in 1 PACKAGE / 2 mL in 1 APPLICATOR (70635-0003-3)
Product Details
What is NDC 70635-0003?
What are the uses for Lutooth Tooth Whitening Kit?
Which are Lutooth Tooth Whitening Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
Which are Lutooth Tooth Whitening Kit 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)
What is the NDC to RxNorm Crosswalk for Lutooth Tooth Whitening Kit?
- RxCUI: 1653115 - carbamide peroxide 15 % Oral Gel
- RxCUI: 1653115 - carbamide peroxide 0.15 MG/MG Oral Gel
- RxCUI: 1653115 - carbamide peroxide 15 % 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".