Puristic
NDC Package 82422-001-01

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.

Puristic is ■ tap lightly downward, gently bend the dot of ampoule ■ content turn yellow, to activate and emit through the body surface ■ content turn white, to be discarded in regular trash. Marketed by Medi K Co., Ltd., this product is identified by NDC 82422-001.

Identification & Billing

NDC Package Code
82422-001-01
Package Description
6 mL in 1 BOTTLE
Product Code
82422-001
11-Digit Billing Format
82422000101

Clinical Specifications

Proprietary Name
Puristic
Dosage Form
-
Usage Information
■ tap lightly downward, gently bend the dot of ampoule ■ content turn yellow, to activate and emit through the body surface ■ content turn white, to be discarded in regular trash

Regulatory & Marketing

Labeler Name
Medi K Co., 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
11-27-2021
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 82422-001-01 identifies a specific commercial package of 6 ml in 1 bottle of Puristic, labeled by Medi K Co., 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 Medi K Co., Ltd. on November 27, 2021. The current certification is valid through December 31, 2022.

How is this Medi K Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82422000101. 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)
82422-001-01
11-Digit CMS (5-4-2)
82422-0001-01

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