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  4. NDC Product Code: 80371-102 Biolustre Hygienic Hand Cleaning Wipes

NDC 80371-102 Biolustre Hygienic Hand Cleaning Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 80371-102?
  5. Biolustre Hygienic Hand Cleaning 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:
80371-102
Proprietary Name:
Biolustre Hygienic Hand Cleaning Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Koyuncu Bilisim Teknolojileri Sanayi Ve Ticaret Limited Sirketi
Labeler Code:
80371
Product Label ID:
ae3777da-1860-b6f1-e053-2a95a90af086
Start Marketing Date: [9]
08-31-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Shape:
SQUARE (C48350)

Product Packages

NDC Code 80371-102-01

Package Description: 1 g in 1 POUCH

Product Details

What is NDC 80371-102?

The NDC code 80371-102 is assigned by the FDA to the product Biolustre Hygienic Hand Cleaning Wipes which is product labeled by Koyuncu Bilisim Teknolojileri Sanayi Ve Ticaret Limited Sirketi. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80371-102-01 1 g 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 Biolustre Hygienic Hand Cleaning Wipes?

Used for antibacterial hand skin, prevent bacteria.

Which are Biolustre Hygienic Hand Cleaning Wipes UNII Codes?

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

Which are Biolustre Hygienic Hand Cleaning 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".