Vitaplus Fore
NDC Package 71544-0022-1

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

Vitaplus Fore is do not dilute.• Use at strength for maximum effectiveness.• For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab. Marketed by My Corp.,ltd, this product is identified by NDC 71544-0022.

Identification & Billing

NDC Package Code
71544-0022-1
Package Description
4000 mL in 1 DRUM
Product Code
71544-0022
11-Digit Billing Format
71544002201

Clinical Specifications

Proprietary Name
Vitaplus Fore
Dosage Form
-
Usage Information
Do not dilute.• Use at strength for maximum effectiveness.• For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

Regulatory & Marketing

Labeler Name
My Corp.,ltd
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
04-01-2021
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 71544-0022-1 identifies a specific commercial package of 4000 ml in 1 drum of Vitaplus Fore, labeled by My Corp.,ltd. 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 My Corp.,ltd on April 01, 2021. The current certification is valid through December 31, 2022.

How is this My Corp.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71544002201. 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)
71544-0022-1
11-Digit CMS (5-4-2)
71544-0022-01

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