Chemcor Chemical Foaming Hand Sanitizer Liquid
NDC Package 68041-519-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Chemcor Chemical Foaming Hand Sanitizer (benzalkonium chloride) liquids is pump a small amount of foam into palm of handRub thoroughly over all surfaces of both handsRub hands together briskly until dry. This formulation utilizes a liquid delivery system. Marketed by Chemcor Chemical Corporation, this product is identified by NDC 68041-519 and is authorized under FDA application M.

Identification & Billing

NDC Package Code
68041-519-00
Package Description
4 BOTTLE in 1 BOX / 3785 mL in 1 BOTTLE (68041-519-01)
Product Code
68041-519
11-Digit Billing Format
68041051900
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Chemcor Chemical Foaming Hand Sanitizer
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
BENZALKONIUM CHLORIDE .0013 mg/mL
Usage Information
Pump a small amount of foam into palm of handRub thoroughly over all surfaces of both handsRub hands together briskly until dry

Regulatory & Marketing

Labeler Name
Chemcor Chemical Corporation
Product Type
Human Otc Drug
FDA Application #
M
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2020
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 68041-519-00 identifies a specific commercial package of 4 bottle in 1 box / 3785 ml in 1 bottle (68041-519-01) of Chemcor Chemical Foaming Hand Sanitizer, a human over the counter drug labeled by Chemcor Chemical Corporation. 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 Chemcor Chemical Corporation on June 01, 2020. The current certification is valid through December 31, 2026.

How is this Chemcor Chemical Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68041051900. 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)
68041-519-00
11-Digit CMS (5-4-2)
68041-0519-00

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