Zuklean Advance 62 Ethyl Alcohol Hand Sanitizer Gel
NDC Package 81814-001-05

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Zuklean Advance 62 Ethyl Alcohol Hand Sanitizer Gel is wet hands thoroughly with product and allow to dry without wiping. Marketed by Grupo Zuker S.a. De C.v., this product is identified by NDC 81814-001 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
81814-001-05
Package Description
500 mL in 1 BOTTLE
Product Code
81814-001
11-Digit Billing Format
81814000105
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Zuklean Advance 62 Ethyl Alcohol Hand Sanitizer Gel
Dosage Form
-
Usage Information
Wet hands thoroughly with product and allow to dry without wiping

Regulatory & Marketing

Labeler Name
Grupo Zuker S.a. De C.v.
FDA Application #
part333E
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
03-15-2021
Listing Expiration
12-31-2022
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 81814-001-05 identifies a specific commercial package of 500 ml in 1 bottle of Zuklean Advance 62 Ethyl Alcohol Hand Sanitizer Gel, labeled by Grupo Zuker S.a. De C.v.. 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 Grupo Zuker S.a. De C.v. on March 15, 2021. The current certification is valid through December 31, 2022.

How is this Grupo Zuker S.a. De C.v. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81814000105. 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)
81814-001-05
11-Digit CMS (5-4-2)
81814-0001-05

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