Sanaux Hand Sanitizer Antibacterial Gel
NDC Package 75509-001-07

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

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

Sanaux Hand Sanitizer Antibacterial Gel is place enough product in your palm to thoroughly cover both hands. Marketed by Sanloz Group Inc., this product is identified by NDC 75509-001 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
75509-001-07
Package Description
250 mL in 1 TUBE
Product Code
75509-001
11-Digit Billing Format
75509000107
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sanaux Hand Sanitizer Antibacterial Gel
Dosage Form
-
Usage Information
Place enough product in your palm to thoroughly cover both hands. Rub hand together briskly until dry. Children under 6 years of age should be supervised when using this product.

Regulatory & Marketing

Labeler Name
Sanloz Group 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
04-15-2020
Listing Expiration
12-31-2021
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (75509-001). Click a package code to view its specific billing and regulatory data.

75509-001-01
30 mL in 1 TUBE
75509-001-02
50 mL in 1 TUBE
75509-001-03
60 mL in 1 TUBE
75509-001-04
100 mL in 1 TUBE
75509-001-05
200 mL in 1 TUBE
75509-001-06
240 mL in 1 TUBE
75509-001-08
500 mL in 1 TUBE
75509-001-09
900 mL in 1 TUBE
75509-001-10
1000 mL in 1 TUBE
75509-001-11
1890 mL in 1 TUBE
75509-001-12
3780 mL in 1 TUBE
75509-001-13
18900 mL in 1 TUBE
75509-001-14
200000 mL in 1 TUBE
75509-001-15
1000000 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 75509-001-07 identifies a specific commercial package of 250 ml in 1 tube of Sanaux Hand Sanitizer Antibacterial Gel, labeled by Sanloz Group 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 Sanloz Group Inc. on April 15, 2020. The current certification is valid through December 31, 2021.

How is this Sanloz Group Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 75509000107. 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)
75509-001-07
11-Digit CMS (5-4-2)
75509-0001-07

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