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  4. NDC Product Code: 49410-200 Teeth Desensitizing And Remineralizing Gel

NDC 49410-200 Teeth Desensitizing And Remineralizing Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49410-200?
  4. Teeth Desensitizing And Remineralizing Gel 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:
49410-200
Proprietary Name:
Teeth Desensitizing And Remineralizing Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fuzhou Difeng Bio-tech Co., Ltd.
Labeler Code:
49410
Product Label ID:
2d4e6542-faa9-63f2-e054-00144ff8d46c
Start Marketing Date: [9]
03-07-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 49410-200?

The NDC code 49410-200 is assigned by the FDA to the product Teeth Desensitizing And Remineralizing Gel which is product labeled by Fuzhou Difeng Bio-tech Co., Ltd.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 49410-200-01 5 container in 1 carton / 200 vial, single-use in 1 container / 1.5 g in 1 vial, single-use, 49410-200-02 5 container in 1 carton / 100 vial, single-use in 1 container / 2 g in 1 vial, single-use, 49410-200-03 5 container in 1 carton / 100 vial, single-use in 1 container / 4 g in 1 vial, single-use, 49410-200-04 5 container in 1 carton / 80 vial, single-use in 1 container / 6 g in 1 vial, single-use, 49410-200-05 6 container in 1 carton / 300 vial, single-use in 1 container / 4.5 g in 1 vial, single-use, 49410-200-06 6 container in 1 carton / 200 vial, single-use in 1 container / 10 g in 1 vial, single-use, 49410-200-07 6 container in 1 carton / 333 vial, single-use in 1 container / 3 g in 1 vial, single-use, 49410-200-08 300 vial, single-use in 1 carton / 3.5 g in 1 vial, single-use. 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 Teeth Desensitizing And Remineralizing Gel?

Adults and children 18 years of age and older: Directly apply 1ml-1.5ml of the product on sensitive teeth, or use it in a custom mouth tray. Keep your mouth open for 10-15 mins. Then rinse your month to clean the gel. Use it 1-2 times daily or as recommended by a dentist or physician. Children under 18 years of age and pregnant, breast feeding women: consult a dentist or physician prior to use.

Which are Teeth Desensitizing And Remineralizing Gel UNII Codes?

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

Which are Teeth Desensitizing And Remineralizing Gel 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 Teeth Desensitizing And Remineralizing Gel?

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: 1038841 - potassium nitrate 5 % / sodium fluoride 0.15 % Toothpaste
  • RxCUI: 1038841 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - pot nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG gel Toothpaste
  • RxCUI: 1038841 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste

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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".