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NDC 79428-010 Cheee Gold Plus Tooth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79428-010?
  4. Cheee Gold Plus Tooth Uses
  5. Active Ingredients UNII Codes
  6. 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:
79428-010
Proprietary Name:
Cheee Gold Plus Tooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nature Plus
Labeler Code:
79428
Product Label ID:
4fa6065b-c0a3-4a3f-98f3-fdfd7408ffae
Start Marketing Date: [9]
07-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 79428-010?

The NDC code 79428-010 is assigned by the FDA to the product Cheee Gold Plus Tooth which is product labeled by Nature Plus. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79428-010-02 1 tube in 1 carton / 130 g in 1 tube (79428-010-01). 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 Cheee Gold Plus Tooth?

Apply product onto a toothbrush and brush teeth. Use a smaller amount than other toothpaste for children or those more sensitive to taste. Keep the lid closed after each use. Brush teeth for 3 minutes or longer with Cheee Gold Toothpaste for better results.

Which are Cheee Gold Plus Tooth UNII Codes?

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

Which are Cheee Gold Plus Tooth 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:

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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".