Moistie Fill Plus
NDC Package 71609-0002-1

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 Fill Plus is after cleansing, apply your skin softner. Marketed by Purecell Korea Co., Ltd., this product is identified by NDC 71609-0002.

Identification & Billing

NDC Package Code
71609-0002-1
Package Description
10 mL in 1 SYRINGE, PLASTIC
Product Code
71609-0002
11-Digit Billing Format
71609000201

Clinical Specifications

Proprietary Name
Moistie Fill Plus
Dosage Form
-
Usage Information
After cleansing, apply your skin softner. Apply an appropriate amount FILL PLUS along your face skin's texture. After 10 to 15 minutes with the FILL PLUS on your face and Finish with your lotion or cream.

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
10-02-2018
Listing Expiration
12-31-2019
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 71609-0002-1 identifies a specific commercial package of 10 ml in 1 syringe, plastic of Moistie Fill Plus, 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 October 02, 2018. The current certification is valid through December 31, 2019.

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: 71609000201. 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)
71609-0002-1
11-Digit CMS (5-4-2)
71609-0002-01

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