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  5. NDC Package Code: 42719-346-50 Byotrol Antibacterial Foaming Hand Sanitizer

NDC Package 42719-346-50 Byotrol Antibacterial Foaming Hand Sanitizer

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
42719-346-50
Package Description:
500 mL in 1 BOTTLE
Product Code:
42719-346
Proprietary Name:
Byotrol Antibacterial Foaming Hand Sanitizer
Usage Information:
UsesFor hand sanitizing to decrease bacteria on the skinRecommended for repeated use
11-Digit NDC Billing Format:
42719034650
NDC to RxNorm Crosswalk:
  • RxCUI: 1020365 - benzalkonium chloride 0.13 % Topical Foam
  • RxCUI: 1020365 - benzalkonium chloride 1.3 MG/ML Topical Foam
    • Labeler Name:
    Byotrol, Inc.
    Sample Package:
    No
    Start Marketing Date:
    03-08-2013
    Listing Expiration Date:
    12-31-2017
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    42719-346-061250 mL in 1 CARTRIDGE
    42719-346-51210 mL in 1 BOTTLE
    42719-346-9950 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 42719-346-50?

    The NDC Packaged Code 42719-346-50 is assigned to a package of 500 ml in 1 bottle of Byotrol Antibacterial Foaming Hand Sanitizer, labeled by Byotrol, Inc.. The product's dosage form is and is administered via form.

    Is NDC 42719-346 included in the NDC Directory?

    No, Byotrol Antibacterial Foaming Hand Sanitizer with product code 42719-346 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Byotrol, Inc. on March 08, 2013 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 42719-346-50?

    The 11-digit format is 42719034650. 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
    5-3-242719-346-505-4-242719-0346-50