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  4. NDC Product Code: 74155-111 Hand Sanitizer Biokaab

NDC 74155-111 Hand Sanitizer Biokaab

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74155-111?
  4. Hand Sanitizer Biokaab 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:
74155-111
Proprietary Name:
Hand Sanitizer Biokaab
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biokaab Inc
Labeler Code:
74155
Product Label ID:
a17e30ed-8b2d-d2b8-e053-2a95a90a64b7
Start Marketing Date: [9]
03-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 74155-111?

The NDC code 74155-111 is assigned by the FDA to the product Hand Sanitizer Biokaab which is product labeled by Biokaab Inc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 74155-111-07 50 ml in 1 bottle, spray , 74155-111-08 236 ml in 1 bottle, spray , 74155-111-19 20000 ml in 1 drum , 74155-111-20 200000 ml in 1 drum , 74155-111-38 3785 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 Hand Sanitizer Biokaab?

Place enough product on hands to cover all surfaces. Rub hands to get her until dry.See the image below:

Which are Hand Sanitizer Biokaab UNII Codes?

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

Which are Hand Sanitizer Biokaab 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".