Lycoris Rubus Whitening Fluid
NDC Package 60778-040-01

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.

Lycoris Rubus Whitening Fluid is indications and usage: 1. Marketed by Lycoris Co., Ltd., this product is identified by NDC 60778-040 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
60778-040-01
Package Description
135 mL in 1 CARTON
Product Code
60778-040
11-Digit Billing Format
60778004001

Clinical Specifications

Proprietary Name
Lycoris Rubus Whitening Fluid
Dosage Form
-
Usage Information
Indications and usage: 1. Tighten the lid after using it. 2. Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight. 3. Use it in the evening after washing face.

Regulatory & Marketing

Labeler Name
Lycoris 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
09-01-2013
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 60778-040-01 identifies a specific commercial package of 135 ml in 1 carton of Lycoris Rubus Whitening Fluid, labeled by Lycoris 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 Lycoris Co., Ltd. on September 01, 2013. The current certification is valid through December 31, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 60778004001. 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)
60778-040-01
11-Digit CMS (5-4-2)
60778-0040-01

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