Antimicrobial Face Body Wash Liquid
NDC Package 37945-902-08

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

Antimicrobial Face Body Wash (benzethonium chloride liquid) liquids is wet hands and other areas to be treated. This formulation utilizes a liquid delivery system. Marketed by Bio-medical & Pharmaceutical Manufacturing Corporation, this product is identified by NDC 37945-902 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
37945-902-08
Package Description
236 g in 1 BOTTLE
Product Code
37945-902
11-Digit Billing Format
37945090208
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Antimicrobial Face Body Wash
Non-Proprietary Name
Benzethonium Chloride Liquid
Substance Name
Benzethonium Chloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
Usage Information
Wet hands and other areas to be treated. Place a small amount of gel in your hands and work into lather. Apply lather to areas to be treated using a gentle, circular motion. Rinse clean.

Regulatory & Marketing

Labeler Name
Bio-medical & Pharmaceutical Manufacturing Corporation
Product Type
Human Otc Drug
FDA Application #
part333E
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
10-09-2015
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 (37945-902). Click a package code to view its specific billing and regulatory data.

37945-902-11
181436 g in 1 DRUM
37945-902-12
18144 g in 1 PAIL

* 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 37945-902-08 identifies a specific commercial package of 236 g in 1 bottle of Antimicrobial Face Body Wash, a human over the counter drug labeled by Bio-medical & Pharmaceutical Manufacturing Corporation. This liquid is formulated for topical use and contains benzethonium 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 Bio-medical & Pharmaceutical Manufacturing Corporation on October 09, 2015. The current certification is valid through December 31, 2026.

How is this Bio-medical & Pharmaceutical Manufacturing Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37945090208. 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)
37945-902-08
11-Digit CMS (5-4-2)
37945-0902-08

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