Belucie Luxury Timeless Golden Age Emulsion
NDC Package 50410-040-01

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.

Belucie Luxury Timeless Golden Age Emulsion is indication and usage1. Marketed by Kimjeongmoon Aloe Co., Ltd., this product is identified by NDC 50410-040 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
50410-040-01
Package Description
125 mL in 1 CARTON
Product Code
50410-040
11-Digit Billing Format
50410004001

Clinical Specifications

Proprietary Name
Belucie Luxury Timeless Golden Age Emulsion
Dosage Form
-
Usage Information
Indication and usage1. Recap the bottle after use.2. Avoid exposure to a high or low temperature of direct sunlight

Regulatory & Marketing

Labeler Name
Kimjeongmoon Aloe Co., Ltd.
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-01-2012
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 50410-040-01 identifies a specific commercial package of 125 ml in 1 carton of Belucie Luxury Timeless Golden Age Emulsion, labeled by Kimjeongmoon Aloe 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 Kimjeongmoon Aloe Co., Ltd. on June 01, 2012. The current certification is valid through December 31, 2018.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50410004001. 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)
50410-040-01
11-Digit CMS (5-4-2)
50410-0040-01

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