Aluminum Zirconium Tetrachlorohydrex Gly Solution
NDC Package 65113-2426-1

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 an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Aluminum Zirconium Tetrachlorohydrex Gly solution is a drug for further processing. This formulation utilizes a solution delivery system. Marketed by G.s. Cosmeceutical Usa, Inc., this product is identified by NDC 65113-2426.

Identification & Billing

NDC Package Code
65113-2426-1
Package Description
520000 mL in 1 DRUM
Product Code
65113-2426
11-Digit Billing Format
65113242601

Clinical Specifications

Proprietary Name
Aluminum Zirconium Tetrachlorohydrex Gly
Non-Proprietary Name
Aluminum Zirconium Tetrachlorohydrex Gly
Substance Name
Aluminum Zirconium Tetrachlorohydrex Gly
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Active Ingredient(s)
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 19 g/100mL

Regulatory & Marketing

Labeler Name
G.s. Cosmeceutical Usa, Inc.
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
07-15-2021
Listing Expiration
12-31-2026
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 65113-2426-1 identifies a specific commercial package of 520000 ml in 1 drum of Aluminum Zirconium Tetrachlorohydrex Gly (UNFINISHED drug), drug for further processing labeled by G.s. Cosmeceutical Usa, Inc.. This solution is formulated for use and contains aluminum zirconium tetrachlorohydrex gly 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 G.s. Cosmeceutical Usa, Inc. on July 15, 2021. The current certification is valid through December 31, 2026.

How is this G.s. Cosmeceutical Usa, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 65113242601. 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 (5-4-1)
65113-2426-1
11-Digit CMS (5-4-2)
65113-2426-01

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