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  4. NDC Product Code: 76749-020 Antibacterial Hand Wipes

NDC 76749-020 Antibacterial Hand Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 76749-020?
  5. Antibacterial Hand Wipes 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:
76749-020
Proprietary Name:
Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Karza Med Group, Llc
Labeler Code:
76749
Product Label ID:
a49a6a82-f28c-e2e2-e053-2a95a90a564c
Start Marketing Date: [9]
07-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Shape:
SQUARE (C48350)

Product Packages

NDC Code 76749-020-02

Package Description: 24 g in 1 BAG

Product Details

What is NDC 76749-020?

The NDC code 76749-020 is assigned by the FDA to the product Antibacterial Hand Wipes which is product labeled by Karza Med Group, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76749-020-02 24 g in 1 bag . 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 Hand Wipes?

For Hand Sanitizing and Decreasing Bacteria on Hands. If irritation occurs stop usage.

Which are Antibacterial Hand Wipes UNII Codes?

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

Which are Antibacterial Hand 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".