1. Home
  2. Labeler Index
  3. Tecozyme Inc
  4. NDC Product Code: 79717-0011 Bad Breath Killer

NDC 79717-0011 Bad Breath Killer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79717-0011?
  4. Bad Breath Killer 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:
79717-0011
Proprietary Name:
Bad Breath Killer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tecozyme Inc
Labeler Code:
79717
Product Label ID:
18390af7-0faa-498f-89e3-1fea263aaf2d
Start Marketing Date: [9]
08-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79717-0011?

The NDC code 79717-0011 is assigned by the FDA to the product Bad Breath Killer which is product labeled by Tecozyme Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79717-0011-2 14 pouch in 1 carton / 84.5 mg in 1 pouch (79717-0011-1). 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 Bad Breath Killer?

■ Use 1 strip per day or per night.■ Fold and apply to upper molar gum surface■ Do not push the strips with tongue for 10 second once applied.■ Safe to use overnight

Which are Bad Breath Killer UNII Codes?

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

Which are Bad Breath Killer 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".