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  5. NDC Package Code: 79761-101-80 Universal Antibacterial Wipes

NDC Package 79761-101-80 Universal Antibacterial Wipes

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
79761-101-80
Package Description:
1 POUCH in 1 BOX / 80 PACKAGE in 1 POUCH / 3.75 mL in 1 PACKAGE
Product Code:
79761-101
Proprietary Name:
Universal Antibacterial Wipes
Usage Information:
To Dispense: Pull-up the lid placed on top of the pouch. Tear straight across to open. Pull first wipe from center of the pouch opening. For use: Gently pull wipe from the center of the pouch. Wipe your hands and skin thoroughly with wipe and let dry. Discard wipe in trash.
11-Digit NDC Billing Format:
79761010180
NDC to RxNorm Crosswalk:
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
    • Labeler Name:
    Monna Kimya Ve Kozmetik Sanayi Ticaret Limited Sirketi
    Sample Package:
    No
    Start Marketing Date:
    07-23-2020
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 79761-101-80?

    The NDC Packaged Code 79761-101-80 is assigned to a package of 1 pouch in 1 box / 80 package in 1 pouch / 3.75 ml in 1 package of Universal Antibacterial Wipes, labeled by Monna Kimya Ve Kozmetik Sanayi Ticaret Limited Sirketi. The product's dosage form is and is administered via form.

    Is NDC 79761-101 included in the NDC Directory?

    No, Universal Antibacterial Wipes with product code 79761-101 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Monna Kimya Ve Kozmetik Sanayi Ticaret Limited Sirketi on July 23, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 79761-101-80?

    The 11-digit format is 79761010180. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-279761-101-805-4-279761-0101-80