Antibe Beausenne Special Ampoule
NDC Package 70929-0002-2

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.

Antibe Beausenne Special Ampoule is after cleansing, apply an appropriate amount of product on the face and neck area and gently pat for absorption. Marketed by Modongee Co., Ltd., this product is identified by NDC 70929-0002.

Identification & Billing

NDC Package Code
70929-0002-2
Package Description
4 BOTTLE, DROPPER in 1 BOX / 50 mL in 1 BOTTLE, DROPPER (70929-0002-1)
Product Code
11-Digit Billing Format
70929000202

Clinical Specifications

Proprietary Name
Antibe Beausenne Special Ampoule
Dosage Form
-
Usage Information
After cleansing, apply an appropriate amount of product on the face and neck area and gently pat for absorption. Use twice daily as the first step of your morning and night skin care regimen.

Regulatory & Marketing

Labeler Name
Modongee 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
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 70929-0002-2 identifies a specific commercial package of 4 bottle, dropper in 1 box / 50 ml in 1 bottle, dropper (70929-0002-1) of Antibe Beausenne Special Ampoule, labeled by Modongee 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 Modongee Co., Ltd. on July 01, 2015. The current certification is valid through December 31, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70929000202. 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)
70929-0002-2
11-Digit CMS (5-4-2)
70929-0002-02

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