Mu Lab Turn Around 2w Refresh Ex
NDC Package 71164-020-02

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.

Mu Lab Turn Around 2w Refresh Ex is directions: - Clean the skin thoroughly before using - Day and night, apply amount of one pumping onto forehead and nose, and massage in the order of forehead, nose->cheeks->eyes. Marketed by Mu-biz.co,.ltd, this product is identified by NDC 71164-020.

Identification & Billing

NDC Package Code
71164-020-02
Package Description
1 TUBE in 1 CARTON / 20 mL in 1 TUBE (71164-020-01)
Product Code
71164-020
11-Digit Billing Format
71164002002

Clinical Specifications

Proprietary Name
Mu Lab Turn Around 2w Refresh Ex
Dosage Form
-
Usage Information
Directions: - Clean the skin thoroughly before using - Day and night, apply amount of one pumping onto forehead and nose, and massage in the order of forehead, nose->cheeks->eyes. The active ingredients are highly concentrated and need to be controlled in this way. The first area to come in contact with this product will be the most effected. So, for instance, apply the designated amount first around the eyes may irritate. Massage lightly. If no irritation is visible, increase amount through a 3-to-4-day interval.

Regulatory & Marketing

Labeler Name
Mu-biz.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
12-01-2016
Listing Expiration
12-31-2017
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 71164-020-02 identifies a specific commercial package of 1 tube in 1 carton / 20 ml in 1 tube (71164-020-01) of Mu Lab Turn Around 2w Refresh Ex, labeled by Mu-biz.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 Mu-biz.co,.ltd on December 01, 2016. The current certification is valid through December 31, 2017.

How is this Mu-biz.co,.ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71164002002. 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)
71164-020-02
11-Digit CMS (5-4-2)
71164-0020-02

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