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  4. NDC Product Code: 75139-005 Ancos Silver Ion Antibacterial

NDC 75139-005 Ancos Silver Ion Antibacterial

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75139-005?
  4. Ancos Silver Ion Antibacterial 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:
75139-005
Proprietary Name:
Ancos Silver Ion Antibacterial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Anson Bio-technology Co., Ltd.
Labeler Code:
75139
Product Label ID:
a4526c53-6477-e4f8-e053-2a95a90a93a7
Start Marketing Date: [9]
04-28-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75139-005-01

Package Description: 100 mL in 1 BOTTLE

Product Details

What is NDC 75139-005?

The NDC code 75139-005 is assigned by the FDA to the product Ancos Silver Ion Antibacterial which is product labeled by Anson Bio-technology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75139-005-01 100 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 Ancos Silver Ion Antibacterial?

Open cap and spray on the skin surface where anti-(suppressing)bacteria is needed and dry naturally without washing again

Which are Ancos Silver Ion Antibacterial UNII Codes?

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

Which are Ancos Silver Ion Antibacterial 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".