Moistie Pure Essence
NDC Package 71609-0004-1

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.

Moistie Pure Essence is apply daily to your cleansed skin.Pure Essence can be attached to the Moistie Skin Therapy Steamer and used together with steam to make the skin clear and clean. Marketed by Purecell Korea Co., Ltd., this product is identified by NDC 71609-0004.

Identification & Billing

NDC Package Code
71609-0004-1
Package Description
3 VIAL in 1 PACKAGE / 10 mL in 1 VIAL
Product Code
71609-0004
11-Digit Billing Format
71609000401

Clinical Specifications

Proprietary Name
Moistie Pure Essence
Dosage Form
-
Usage Information
Apply daily to your cleansed skin.Pure Essence can be attached to the Moistie Skin Therapy Steamer and used together with steam to make the skin clear and clean.

Regulatory & Marketing

Labeler Name
Purecell Korea 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
06-01-2017
Listing Expiration
12-31-2018
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 71609-0004-1 identifies a specific commercial package of 3 vial in 1 package / 10 ml in 1 vial of Moistie Pure Essence, labeled by Purecell Korea 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 Purecell Korea Co., Ltd. on June 01, 2017. The current certification is valid through December 31, 2018.

How is this Purecell Korea Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71609000401. 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)
71609-0004-1
11-Digit CMS (5-4-2)
71609-0004-01

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