Doc Johnson Prolonging Ginseng
NDC Package 69503-003-01

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.

Doc Johnson Prolonging Ginseng is apply a small amount to head and shaft of penis 2-3 minutes before intercourse or use as directed by a physician.Wash product off after intercourse. Marketed by Health Devices Corporation, this product is identified by NDC 69503-003 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
69503-003-01
Package Description
56 g in 1 TUBE
Product Code
69503-003
11-Digit Billing Format
69503000301

Clinical Specifications

Proprietary Name
Doc Johnson Prolonging Ginseng
Dosage Form
-
Usage Information
Apply a small amount to head and shaft of penis 2-3 minutes before intercourse or use as directed by a physician.Wash product off after intercourse.

Regulatory & Marketing

Labeler Name
Health Devices Corporation
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-23-2023
Listing Expiration
12-31-2024
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 69503-003-01 identifies a specific commercial package of 56 g in 1 tube of Doc Johnson Prolonging Ginseng, labeled by Health Devices Corporation. 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 Health Devices Corporation on May 23, 2023. The current certification is valid through December 31, 2024.

How is this Health Devices Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69503000301. 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)
69503-003-01
11-Digit CMS (5-4-2)
69503-0003-01

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