70% Alcohol Hand Sanitizer
NDC Package 50865-074-41

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.

70% Alcohol Hand Sanitizer is for handwashing to help reduce bacteria on the skin.Avoid contact with eyes. Marketed by Kutol Products Company, Inc., this product is identified by NDC 50865-074 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
50865-074-41
Package Description
6 BAG in 1 PACKET / 1000 mL in 1 BAG
Product Code
50865-074
11-Digit Billing Format
50865007441
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
70% Alcohol Hand Sanitizer
Dosage Form
-
Usage Information
For handwashing to help reduce bacteria on the skin.Avoid contact with eyes. If eye contact occurs, flush eyes with water.Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.Keep out of reach of children. If swallowed, contact a physician or poison control center.

Regulatory & Marketing

Labeler Name
Kutol Products Company, 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
02-27-2018
Listing Expiration
12-31-2020
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 (50865-074). Click a package code to view its specific billing and regulatory data.

50865-074-44
4 BAG in 1 PACKET / 1000 mL in 1 BAG

* 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 50865-074-41 identifies a specific commercial package of 6 bag in 1 packet / 1000 ml in 1 bag of 70% Alcohol Hand Sanitizer, labeled by Kutol Products Company, 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 Kutol Products Company, Inc. on February 27, 2018. The current certification is valid through December 31, 2020.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50865007441. 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)
50865-074-41
11-Digit CMS (5-4-2)
50865-0074-41

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