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  4. NDC Product Code: 51289-400 Fluoride Gel

NDC 51289-400 Fluoride Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51289-400?
  4. Fluoride 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:
51289-400
Proprietary Name:
Fluoride Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yangzhou Hengyuan Daily Chemical Plastic Co.,ltd
Labeler Code:
51289
Product Label ID:
33ab7045-39e6-3066-e054-00144ff88e88
Start Marketing Date: [9]
05-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 51289-400?

The NDC code 51289-400 is assigned by the FDA to the product Fluoride Gel which is product labeled by Yangzhou Hengyuan Daily Chemical Plastic Co.,ltd. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 51289-400-01 720 tube in 1 box / 17 g in 1 tube, 51289-400-02 720 tube in 1 box / 24 g in 1 tube, 51289-400-03 144 tube in 1 box / 43 g in 1 tube, 51289-400-04 1000 tube in 1 box / .22 g in 1 tube, 51289-400-05 1000 tube in 1 box / 7 g in 1 tube. 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 Fluoride Gel?

Adults and children 2years of age and older:Brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by a dentist or a physician.Children 2-6 years:Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)Children under 2 years:Ask a dentist or a physician.

Which are Fluoride Gel UNII Codes?

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

Which are Fluoride 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 Fluoride 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:

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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".