Foamfresh E-2 Sanitizer Cleanser Liquid
NDC Package 11429-1002-9
Package Information
Foamfresh E-2 Sanitizer Cleanser (benzalkonium chloride) liquids is uses:For hand washing to decrease bacteria on the skin.Recommended for repeated use. This formulation utilizes a liquid delivery system. Marketed by Woodbine Products Company, this product is identified by NDC 11429-1002 and is authorized under FDA application 505G(a)(3).
Identification & Billing
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 11429 - Woodbine Products Company
- 11429-1002 - Foamfresh E-2 Sanitizer Cleanser
- 11429-1002-9 - 1100 mL in 1 BOTTLE
- 11429-1002 - Foamfresh E-2 Sanitizer Cleanser
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 (11429-1002). 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 11429-1002-9 identifies a specific commercial package of 1100 ml in 1 bottle of Foamfresh E-2 Sanitizer Cleanser, a human over the counter drug labeled by Woodbine Products Company. This liquid is formulated for topical 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 Woodbine Products Company on February 26, 2014. The current certification is valid through December 31, 2026.
How is this Woodbine Products Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 11429100209. 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 Package segment to maintain the 5-4-2 structure.