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  4. NDC Product Code: 79258-107 Antibacterial Wipes

NDC 79258-107 Antibacterial Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79258-107?
  4. Antibacterial Wipes 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:
79258-107
Proprietary Name:
Antibacterial Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Brady Industries, Inc.
Labeler Code:
79258
Product Label ID:
aa88ddc7-36c5-4570-e053-2995a90a2710
Start Marketing Date: [9]
07-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79258-107-20

Package Description: .1 mL in 1 CANISTER

Product Details

What is NDC 79258-107?

The NDC code 79258-107 is assigned by the FDA to the product Antibacterial Wipes which is product labeled by Brady Industries, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79258-107-20 .1 ml in 1 canister . 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 Antibacterial Wipes?

Wet hands thoroughlly with product and allow to dryChildren under 6 years of age should be supervised with using this product.

Which are Antibacterial Wipes UNII Codes?

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

Which are Antibacterial Wipes 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".