Sani Luxe Foaming Hand Sanitizer Alcohol Free Liquid
NDC Package 71489-006-06
Package Information
Sani Luxe Foaming Hand Sanitizer Alcohol Free (benzalkonium chloride) liquids is pump a small amount of foam into palm of handRub hands together briskly until dryRub thoroughly over all surfaces of both hands. This formulation utilizes a liquid delivery system. Marketed by Celeste Industries Corporation, this product is identified by NDC 71489-006 and is authorized under FDA application 505G(a)(3).
Identification & Billing
- RxCUI: 1038799 - benzalkonium chloride 0.1 % Topical Foam
- RxCUI: 1038799 - benzalkonium chloride 1 MG/ML Topical Foam
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71489 - Celeste Industries Corporation
- 71489-006 - Sani Luxe Foaming Hand Sanitizer Alcohol Free
- 71489-006-06 - 3785 mL in 1 BOTTLE
- 71489-006 - Sani Luxe Foaming Hand Sanitizer Alcohol Free
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 (71489-006). Click a package code to view its specific billing and regulatory data.
* 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 71489-006-06 identifies a specific commercial package of 3785 ml in 1 bottle of Sani Luxe Foaming Hand Sanitizer Alcohol Free, a human over the counter drug labeled by Celeste Industries Corporation. This liquid is formulated for cutaneous use and contains benzalkonium 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 Celeste Industries Corporation on January 28, 2019. The current certification is valid through December 31, 2026.
How is this Celeste Industries Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71489000606. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
