1. Home
  2. Labeler Index
  3. Koji Corporation Co., Ltd
  4. NDC Product Code: 80703-0001 Yesdentok Khurb Clean Disinfection Water

NDC 80703-0001 Yesdentok Khurb Clean Disinfection Water

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80703-0001?
  4. Yesdentok Khurb Clean Disinfection Water 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:
80703-0001
Proprietary Name:
Yesdentok Khurb Clean Disinfection Water
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Koji Corporation Co., Ltd
Labeler Code:
80703
Product Label ID:
b1d551ac-340a-8e37-e053-2995a90ae786
Start Marketing Date: [9]
10-17-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 80703-0001?

The NDC code 80703-0001 is assigned by the FDA to the product Yesdentok Khurb Clean Disinfection Water which is product labeled by Koji Corporation Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80703-0001-1 30 ml in 1 bottle . 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 Yesdentok Khurb Clean Disinfection Water?

Pump a small amount of product into palm of hand, mouth and scraper.Rub thoroughly over all surfaces of both hands for 15 seconds.After using tongue cleaner, spray evenly on the mouth and spit out about 15 seconds later.

Which are Yesdentok Khurb Clean Disinfection Water UNII Codes?

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

Which are Yesdentok Khurb Clean Disinfection Water 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".