Dzeus Climax Control Wipes
NDC Package 54723-006-01

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.

Dzeus Climax Control Wipes is use wipe to apply a small amount of product to the head and shape of the penis before intercourse, or as directed by a doctor. Marketed by Sambria Pharmaceuticals, Llc, this product is identified by NDC 54723-006 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
54723-006-01
Package Description
3 mL in 1 POUCH
Product Code
54723-006
11-Digit Billing Format
54723000601

Clinical Specifications

Proprietary Name
Dzeus Climax Control Wipes
Dosage Form
-
Usage Information
Use wipe to apply a small amount of product to the head and shape of the penis before intercourse, or as directed by a doctor. Was off after intercourse Allow product to dry prior to intercourse Not suitable for oral use Use as directed

Regulatory & Marketing

Labeler Name
Sambria Pharmaceuticals, Llc
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-08-2021
Listing Expiration
12-31-2025
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 54723-006-01 identifies a specific commercial package of 3 ml in 1 pouch of Dzeus Climax Control Wipes, labeled by Sambria Pharmaceuticals, Llc. 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 Sambria Pharmaceuticals, Llc on December 08, 2021. The current certification is valid through December 31, 2025.

How is this Sambria Pharmaceuticals, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54723000601. 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)
54723-006-01
11-Digit CMS (5-4-2)
54723-0006-01

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