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  4. NDC Product Code: 81797-701 Ko-c100

NDC 81797-701 Ko-c100

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 81797-701?
  5. Ko-c100 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:
81797-701
Proprietary Name:
Ko-c100
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dong Fuh Biotech Co., Ltd.
Labeler Code:
81797
Product Label ID:
bf823253-00ce-20d6-e053-2995a90a3fcc
Start Marketing Date: [9]
04-09-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
10 MM
Score:
1
Flavor(s):
EGG NOG (C73387)

Product Packages

NDC Code 81797-701-15

Package Description: 1000 DOSE PACK in 1 PACKAGE / 1 g in 1 DOSE PACK (81797-701-00)

Product Details

What is NDC 81797-701?

The NDC code 81797-701 is assigned by the FDA to the product Ko-c100 which is product labeled by Dong Fuh Biotech Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81797-701-15 1000 dose pack in 1 package / 1 g in 1 dose pack (81797-701-00). 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 Ko-c100?

Take out 1 KO-100C Disinfectant, add it to a container filled with 1000c.c. water, let it stand for 1-3 minutes to dissolve into a light yellow disinfectant stock solution, and then distribute it to various containers for immediate use.

Which are Ko-c100 UNII Codes?

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

Which are Ko-c100 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".