NDC 70635-0003 Lutooth Tooth Whitening Kit

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70635-0003
Proprietary Name:
Lutooth Tooth Whitening Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Quorum Bio Co.,ltd
Labeler Code:
70635
Start Marketing Date: [9]
01-01-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

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?

The NDC code 70635-0003 is assigned by the FDA to the product Lutooth Tooth Whitening Kit which is product labeled by Quorum Bio Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70635-0003-4 2 applicator in 1 package / 2 ml in 1 applicator (70635-0003-3). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Lutooth Tooth Whitening Kit?

Tooth Whitening Procedure & MethodYou can find video clips of 'How to Use' at Lutooth hompage (http://www.lutooth.com)For detailed descriptions, plase refer to the user manual inside the product package. Exercise of installationThe Use of Whitening Stick Put Cotton rollsPut the lip&cheek retractorWipe saliva with the cotton roll Apply whitening gelsInstallation & Operation of LED AcceleratorFinishing 1 Cycle Repeat (Three cycles a day)Turn on LED light without whitening gels (Optional)

Which are Lutooth Tooth Whitening Kit UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Lutooth Tooth Whitening Kit?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[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".