F X Fantacell Ampoule
NDC Package 71081-010-02

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.

F X Fantacell Ampoule is indications & usage: 1. Marketed by Glhkorea, this product is identified by NDC 71081-010 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
71081-010-02
Package Description
16 VIAL in 1 CARTON / 8 mL in 1 VIAL (71081-010-01)
Product Code
11-Digit Billing Format
71081001002

Clinical Specifications

Proprietary Name
F X Fantacell Ampoule
Dosage Form
-
Usage Information
Indications & usage: 1. Please spray an F-X Fantacell Solution Ampoule by using the exclusive spray device (Airbrush Compressor) 2. Fill an Airbrush with a half bottle of an F-X Fantacell Solution Ampoule each time and spray it directly to the body parts such as face, neck, hands, feet, full body and etc.

Regulatory & Marketing

Labeler Name
Glhkorea
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
10-01-2016
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 71081-010-02 identifies a specific commercial package of 16 vial in 1 carton / 8 ml in 1 vial (71081-010-01) of F X Fantacell Ampoule, labeled by Glhkorea. 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 Glhkorea on October 01, 2016. The current certification is valid through December 31, 2018.

How is this Glhkorea product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71081001002. 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)
71081-010-02
11-Digit CMS (5-4-2)
71081-0010-02

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