Bzk Towelette Swab
NDC Package 0924-7112-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Bzk Towelette (benzalkonium chloride) swabs is tear open packet, unfold and use as a washcloth. This formulation utilizes a swab delivery system. Marketed by Acme United Corporation, this product is identified by NDC 0924-7112 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
0924-7112-01
Package Description
10 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
Product Code
0924-7112
11-Digit Billing Format
00924711201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Bzk Towelette
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
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
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)
BENZALKONIUM CHLORIDE 1.33 mg/mL
Usage Information
Tear open packet, unfold and use as a washcloth.

Regulatory & Marketing

Labeler Name
Acme United Corporation
Product Type
Human Otc Drug
FDA Application #
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
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0924-7112). Click a package code to view its specific billing and regulatory data.

0924-7112-00
1.4 mL in 1 POUCH
0924-7112-02
10 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
0924-7112-03
25 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
0924-7112-04
50 POUCH in 1 CARTON / 1.4 mL in 1 POUCH
0924-7112-05
100 POUCH in 1 CARTON / 1.4 mL in 1 POUCH

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0924-7112-01 identifies a specific commercial package of 10 pouch in 1 carton / 1.4 ml in 1 pouch of Bzk Towelette, a human over the counter drug labeled by Acme United Corporation. This swab is formulated for topical use and contains benzalkonium chloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Acme United Corporation on April 16, 2019. The current certification is valid through December 31, 2026.

How is this Acme United Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00924711201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0924-7112-01
11-Digit CMS (5-4-2)
00924-7112-01

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.