Antibacterial Hand
NDC Package 78939-002-01

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.

Antibacterial Hand is wet hands with water, apply soap and rub for 20 seconds and rinse. Marketed by Cross Border Manufacturers Inc., this product is identified by NDC 78939-002 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
78939-002-01
Package Description
500 mL in 1 BOTTLE, PLASTIC
Product Code
78939-002
11-Digit Billing Format
78939000201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Antibacterial Hand
Dosage Form
-
Usage Information
Wet hands with water, apply soap and rub for 20 seconds and rinse.

Regulatory & Marketing

Labeler Name
Cross Border Manufacturers Inc.
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
09-16-2020
Listing Expiration
12-31-2022
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 78939-002-01 identifies a specific commercial package of 500 ml in 1 bottle, plastic of Antibacterial Hand, labeled by Cross Border Manufacturers Inc.. 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 Cross Border Manufacturers Inc. on September 16, 2020. The current certification is valid through December 31, 2022.

How is this Cross Border Manufacturers Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 78939000201. 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)
78939-002-01
11-Digit CMS (5-4-2)
78939-0002-01

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