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  4. NDC Product Code: 47649-1102 Dr.whitiss 15%

NDC 47649-1102 Dr.whitiss 15%

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 47649-1102?
  4. Dr.whitiss 15% Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
47649-1102
Proprietary Name:
Dr.whitiss 15%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nibec Co., Ltd.
Labeler Code:
47649
Product Label ID:
99689ede-29bb-17cb-e053-2995a90a5328
Start Marketing Date: [9]
06-07-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 47649-1102?

The NDC code 47649-1102 is assigned by the FDA to the product Dr.whitiss 15% which is product labeled by Nibec Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 47649-1102-2 4 syringe in 1 package / 1 g in 1 syringe (47649-1102-1). 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 Dr.whitiss 15%?

1. Gingival and general oral heath should be confirmed before treatment. 2. Brush your teeth before treatment. 3. Follow your dentist’s instructions on how to load gel into your custom whitening tray. Use no more than 1/3 to 1/2 of the syringe per tray. 4. Insert whitening tray in the mouth over the teeth. Seat the tray firmly agains the teeth. Remove excess gel with clean finger or soft toothbrush.(Rinse twice; do not swallow rinsed gel.) 5. Unless directed otherwise by your dentist, wear Dr.Whitiss 10% for 8-10 hours or overnight, Dr.Whitiss 15% for 4-6 hours, Dr.Whitiss20% for 2-4 hours, and Dr.Whitiss 35% for 30 minutes. 6. If significant sensitivity occurs, stop treatment and consult dentist.

Which are Dr.whitiss 15% UNII Codes?

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

Which are Dr.whitiss 15% 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 Dr.whitiss 15%?

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:
  • RxCUI: 2265639 - carbamide peroxide 15 % / sodium fluoride 0.25 % Oral Gel
  • RxCUI: 2265639 - carbamide peroxide 0.15 MG/MG / sodium fluoride 0.0025 MG/MG Oral Gel
  • RxCUI: 2265639 - carbamide peroxide 0.15 MG/MG / sodium fluoride 0.0025 MG/MG Dental Gel

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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".