Scrubs Foaming Hand Sanitizer
NDC Package 51239-1929-7

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.

Scrubs Foaming Hand Sanitizer is a medication used as UsesFor hand washing to decrease bacteria on skin.Recommended for repeated use. Marketed by Itw Dymon, this product is identified by NDC 51239-1929 and is authorized under FDA application part333.

Identification & Billing

NDC Package Code
51239-1929-7
Package Description
252 mL in 1 BOTTLE, PUMP
Product Code
51239-1929
11-Digit Billing Format
51239192907
RxNorm Crosswalk
  • RxCUI: 1039014 - benzalkonium Cl 0.1 % / benzethonium chloride l 0.1 % Topical Foam
  • RxCUI: 1039014 - benzalkonium chloride 1 MG/ML / benzethonium chloride 1 MG/ML Topical Foam
  • RxCUI: 1039014 - benzalkonium chloride 0.1 % / benzethonium chloride 0.1 % Topical Foam
  • RxCUI: 1039016 - SCRUBS 0.1 % / 0.1 % Topical Foam
  • RxCUI: 1039016 - benzalkonium chloride 1 MG/ML / benzethonium chloride 1 MG/ML Topical Foam [Scrubs]

Clinical Specifications

Proprietary Name
Scrubs Foaming Hand Sanitizer Scrubs
Dosage Form
-
Usage Information
This product is used as UsesFor hand washing to decrease bacteria on skin.Recommended for repeated use.

Regulatory & Marketing

Labeler Name
Itw Dymon
FDA Application #
part333
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
10-01-2009
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 51239-1929-7 identifies a specific commercial package of 252 ml in 1 bottle, pump of Scrubs Foaming Hand Sanitizer Scrubs, labeled by Itw Dymon. 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 Itw Dymon on October 01, 2009. The current certification is valid through December 31, 2017.

How is this Itw Dymon product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51239192907. 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 (5-4-1)
51239-1929-7
11-Digit CMS (5-4-2)
51239-1929-07

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