Foaming Sanitizing Hand Soap
NDC Package 50865-710-92

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

Foaming Sanitizing Hand (alcohol) soaps is Uses Hand sanitizer to help reduce bacteria on the skin that could cause disease. This formulation utilizes a soap delivery system. Marketed by Kutol Products Company, this product is identified by NDC 50865-710 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
50865-710-92
Package Description
59 mL in 1 BOTTLE
Product Code
50865-710
11-Digit Billing Format
50865071092

Clinical Specifications

Proprietary Name
Foaming Sanitizing Hand
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
ALCOHOL .072 mg/mL
Usage Information
Uses Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Regulatory & Marketing

Labeler Name
Kutol Products Company
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-01-2015
Listing Expiration
12-31-2027
Exclude Flag
N
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 (50865-710). Click a package code to view its specific billing and regulatory data.

50865-710-17
50 mL in 1 BOTTLE, PLASTIC
50865-710-41
1000 mL in 1 BAG
50865-710-44
1000 mL in 1 BAG
50865-710-55
1200 mL in 1 BAG
50865-710-91
532 mL in 1 BOTTLE, PUMP

* 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 50865-710-92 identifies a specific commercial package of 59 ml in 1 bottle of Foaming Sanitizing Hand, a human over the counter drug labeled by Kutol Products Company. This soap is formulated for topical use and contains alcohol 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 Kutol Products Company on October 01, 2015. The current certification is valid through December 31, 2027.

How is this Kutol Products Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50865071092. 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)
50865-710-92
11-Digit CMS (5-4-2)
50865-0710-92

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