NDC Package 0924-7112-05 Bzk Towelette

Benzalkonium Chloride Swab 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:
0924-7112-05
Package Description:
100 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
Product Code:
Proprietary Name:
Bzk Towelette
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Tear open packet, unfold and use as a washcloth.
11-Digit NDC Billing Format:
00924711205
NDC to RxNorm Crosswalk:
  • RxCUI: 1043307 - benzalkonium Cl 0.133 % Medicated Pad
  • RxCUI: 1043307 - benzalkonium chloride 1.33 MG/ML Medicated Pad
  • RxCUI: 1043307 - benzalkonium chloride 0.133 % Medicated Towelette
  • RxCUI: 1043307 - benzalkonium chloride 0.133 % Topical Swab
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Acme United Corporation
    Dosage Form:
    Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
    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:
    part333A
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    04-16-2019
    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
    0924-7112-001.4 mL in 1 POUCH
    0924-7112-0110 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
    0924-7112-0210 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
    0924-7112-0325 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
    0924-7112-0450 POUCH in 1 CARTON / 1.4 mL in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0924-7112-05?

    The NDC Packaged Code 0924-7112-05 is assigned to a package of 100 pouch in 1 carton / 1.4 ml in 1 pouch of Bzk Towelette, a human over the counter drug labeled by Acme United Corporation. The product's dosage form is swab and is administered via topical form.

    Is NDC 0924-7112 included in the NDC Directory?

    Yes, Bzk Towelette with product code 0924-7112 is active and included in the NDC Directory. The product was first marketed by Acme United Corporation on April 16, 2019 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 0924-7112-05?

    The 11-digit format is 00924711205. 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 4-4-2 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
    4-4-20924-7112-055-4-200924-7112-05