Forpro Professional Collection Alcohol-free Foaming Instant Hand Sanitizer Liquid
NDC Package 59555-404-13
Package Information
Forpro Professional Collection Alcohol-free Foaming Instant Hand Sanitizer (benzalkonium chloride) liquids is pump sufficient amount of foam into palm of hand.Wet all surfaces of both hands thoroughly with product, including the area under the fingernails and rub until dry. This formulation utilizes a liquid delivery system. Marketed by R & R Lotion, Inc, this product is identified by NDC 59555-404 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
- 59555 - R & R Lotion, Inc
- 59555-404 - Forpro Professional Collection Alcohol-free Foaming Instant Hand Sanitizer
- 59555-404-13 - 50 mL in 1 BOTTLE, PUMP
- 59555-404 - Forpro Professional Collection Alcohol-free Foaming Instant Hand Sanitizer
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 (59555-404). 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 59555-404-13 identifies a specific commercial package of 50 ml in 1 bottle, pump of Forpro Professional Collection Alcohol-free Foaming Instant Hand Sanitizer, a human over the counter drug labeled by R & R Lotion, Inc. 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 R & R Lotion, Inc on May 28, 2025. The current certification is valid through December 31, 2027.
How is this R & R Lotion, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 59555040413. 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.