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  4. NDC Product Code: 75109-002 Bye Bye Germs Antibacterial Wipes

NDC 75109-002 Bye Bye Germs Antibacterial Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75109-002?
  4. Bye Bye Germs 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:
75109-002
Proprietary Name:
Bye Bye Germs Antibacterial Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kangna (zhejiang) Medical Supplies Co., Ltd.
Labeler Code:
75109
Product Label ID:
6aa2fc38-c077-4b96-81f1-c6c18db56cbf
Start Marketing Date: [9]
10-05-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 75109-002?

The NDC code 75109-002 is assigned by the FDA to the product Bye Bye Germs Antibacterial Wipes which is product labeled by Kangna (zhejiang) Medical Supplies Co., Ltd.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 75109-002-01 75 cloth in 1 pouch , 75109-002-02 75 cloth in 1 canister , 75109-002-03 25 cloth in 1 pouch . 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 Bye Bye Germs Antibacterial Wipes?

Lift tab and pull out towel to wipe hands thoroughly for 30 seconds. Allow to air dry.Reseal after use to prevent moisture from evaporating.Children under 6 years of age should be supervised when using this product.

Which are Bye Bye Germs Antibacterial Wipes UNII Codes?

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

Which are Bye Bye Germs 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".