Benzethonium Chloride Solution
NDC Package 54340-252-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Benzethonium Chloride Solution is for handwashing to decrease bacteria on the skin. Marketed by The Dial Corporation, A Henkel Company, this product is identified by NDC 54340-252 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
54340-252-01
Package Description
221 mL in 1 BOTTLE, PUMP
Product Code
54340-252
11-Digit Billing Format
54340025201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Benzethonium Chloride Solution
Dosage Form
-
Usage Information
For handwashing to decrease bacteria on the skin

Regulatory & Marketing

Labeler Name
The Dial Corporation, A Henkel Company
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
01-05-2015
Listing Expiration
12-31-2017
Exclude Flag
I
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 54340-252-01 identifies a specific commercial package of 221 ml in 1 bottle, pump of Benzethonium Chloride Solution, labeled by The Dial Corporation, A Henkel Company. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by The Dial Corporation, A Henkel Company on January 05, 2015. The current certification is valid through December 31, 2017.

How is this The Dial Corporation, A Henkel Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54340025201. 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)
54340-252-01
11-Digit CMS (5-4-2)
54340-0252-01

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