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  4. NDC Product Code: 80143-001 Fluoride

NDC 80143-001 Fluoride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 80143-001?
  5. Fluoride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80143-001
Proprietary Name:
Fluoride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Henan Dailygreen Trade Co.,ltd.
Labeler Code:
80143
Product Label ID:
ad447c9a-6f0f-7fef-e053-2995a90a055f
Start Marketing Date: [9]
06-24-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - NONE)
Shape:
ROUND (C48348)
Size(s):
11 MM
Flavor(s):
MINT (C73404 - NONE)

Code Structure Chart

Product Details

What is NDC 80143-001?

The NDC code 80143-001 is assigned by the FDA to the product Fluoride which is product labeled by Henan Dailygreen Trade Co.,ltd.. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 80143-001-01 60 tablet, chewable in 1 bottle, glass , 80143-001-02 62 tablet, chewable in 1 bottle, glass , 80143-001-03 120 tablet, chewable in 1 bottle, glass , 80143-001-04 60 tablet, chewable in 1 tube , 80143-001-05 90 tablet, chewable in 1 tube , 80143-001-06 120 tablet, chewable in 1 tube , 80143-001-07 30 tablet, chewable in 1 carton , 80143-001-08 60 tablet, chewable in 1 carton , 80143-001-09 2 tablet, chewable in 1 bag , 80143-001-10 62 tablet, chewable in 1 bag , 80143-001-11 120 tablet, chewable in 1 bag , 80143-001-12 1000 tablet, chewable in 1 bag . 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?

This medication is used to prevent cavities. It makes teeth stronger and more resistant to decay caused by acid and bacteria. Talk to your dentist or doctor about the benefits and risks of this product. This medication is not recommended for use in infants less than 6 months of age. This medication is not recommended for use in areas where the fluoride content in the water supply is greater than 0.6 parts per million. See Notes section for more information.

Which are Fluoride UNII Codes?

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

Which are Fluoride 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:

* Please review the disclaimer below.

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".