Antibacterial Lidocaine Wound Gel
NDC Package 51142-652-28

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

Antibacterial Lidocaine Wound Gel (benzalkonium chloride, lidocaine hydrochloride) gel is clean the affected areaadults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: consult a doctormay be covered with a sterile bandageif bandaged, let dry first. This formulation utilizes a gel delivery system. Marketed by Aso Llc, this product is identified by NDC 51142-652 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
51142-652-28
Package Description
1 TUBE in 1 CARTON / 28 mL in 1 TUBE
Product Code
51142-652
11-Digit Billing Format
51142065228
RxNorm Crosswalk
  • RxCUI: 1431682 - benzalkonium chloride 0.13 % / lidocaine HCl 2 % Topical Gel
  • RxCUI: 1431682 - benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.02 MG/MG Topical Gel
  • RxCUI: 1431682 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 2 % Topical Gel

Clinical Specifications

Proprietary Name
Antibacterial Lidocaine Wound Gel
Non-Proprietary Name
Benzalkonium Chloride, Lidocaine Hydrochloride
Substance Name
Benzalkonium Chloride; Lidocaine Hydrochloride
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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)
Pharmacologic Class
Usage Information
Clean the affected areaadults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: consult a doctormay be covered with a sterile bandageif bandaged, let dry first

Regulatory & Marketing

Labeler Name
Aso Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-28-2019
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 (51142-652). Click a package code to view its specific billing and regulatory data.

51142-652-14
1 TUBE in 1 CARTON / 14 mL in 1 TUBE

* 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 51142-652-28 identifies a specific commercial package of 1 tube in 1 carton / 28 ml in 1 tube of Antibacterial Lidocaine Wound Gel, a human over the counter drug labeled by Aso Llc. This gel is formulated for topical use and contains benzalkonium chloride; lidocaine hydrochloride 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 Aso Llc on October 28, 2019. The current certification is valid through December 31, 2026.

How is this Aso Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51142065228. 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 (5-3-2)
51142-652-28
11-Digit CMS (5-4-2)
51142-0652-28

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