Hyaluronic Acid Micro
NDC Package 70018-010-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Hyaluronic Acid Micro is indications & usage:1. Marketed by Junmok International,inc, this product is identified by NDC 70018-010.

Identification & Billing

NDC Package Code
70018-010-01
Package Description
4 PATCH in 1 CARTON
Product Code
11-Digit Billing Format
70018001001

Clinical Specifications

Proprietary Name
Hyaluronic Acid Micro
Dosage Form
-
Usage Information
Indications & usage:1. Take a patch out of the pouch with dry hand after face washing. 2. Try not to touch the middle side (needle) and take off the protective film carefully. 3. Place and attach the middle side of the patch on a desired area vertically. 4. Press the middle part of the patch attached with fingers several times. 5. Go to bed with patch attached and take it off the next morning.

Regulatory & Marketing

Labeler Name
Junmok International,inc
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
07-01-2015
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 70018-010-01 identifies a specific commercial package of 4 patch in 1 carton of Hyaluronic Acid Micro, labeled by Junmok International,inc. 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 Junmok International,inc on July 01, 2015. The current certification is valid through December 31, 2017.

How is this Junmok International,inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70018001001. 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)
70018-010-01
11-Digit CMS (5-4-2)
70018-0010-01

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