NDC Package 57362-467-02 Zylastxp Antiseptic Foaming

Benzethonium Chloride Soap Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
57362-467-02
Package Description:
1000 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Zylastxp Antiseptic Foaming
Non-Proprietary Name:
Benzethonium Chloride
Substance Name:
Benzethonium Chloride
Usage Information:
Wet hands and forearms. Apply a palmful to hands and scrub hands and forearms thoroughly for 15 seconds or more. Rinse and repeat. Wet hands and forearms. Apply a palmful to hands and scrub hands and forearms thoroughly for 15 seconds or more. Rinse and repeat.
11-Digit NDC Billing Format:
57362046702
NDC to RxNorm Crosswalk:
  • RxCUI: 1243889 - benzethonium chloride 0.2 % Medicated Liquid Soap
  • RxCUI: 1243889 - benzethonium chloride 2 MG/ML Medicated Liquid Soap
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Innovative Biodefense
    Dosage Form:
    Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-06-2015
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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
    57362-467-01244 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57362-467-02?

    The NDC Packaged Code 57362-467-02 is assigned to a package of 1000 ml in 1 bottle of Zylastxp Antiseptic Foaming, a human over the counter drug labeled by Innovative Biodefense. The product's dosage form is soap and is administered via topical form.

    Is NDC 57362-467 included in the NDC Directory?

    Yes, Zylastxp Antiseptic Foaming with product code 57362-467 is active and included in the NDC Directory. The product was first marketed by Innovative Biodefense on April 06, 2015 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 57362-467-02?

    The 11-digit format is 57362046702. 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
    5-3-257362-467-025-4-257362-0467-02