Derma Honey Mask
NDC Package 72312-0010-1

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.

Derma Honey Mask is 1. Marketed by Cellalab, this product is identified by NDC 72312-0010 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
72312-0010-1
Package Description
5 POUCH in 1 PACKAGE / 30 g in 1 POUCH
Product Code
72312-0010
11-Digit Billing Format
72312001001

Clinical Specifications

Proprietary Name
Derma Honey Mask
Dosage Form
-
Usage Information
1. Gently smooth skin texture with toner after cleansing. 2. Remove the film after taking out Derma Honey Mask and place the mask properly on face. 3. After 10-20 minutes, remove the mask and tap the face lightly to allow residual essence to be absorbed.

Regulatory & Marketing

Labeler Name
Cellalab
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
03-01-2018
Listing Expiration
12-31-2019
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 72312-0010-1 identifies a specific commercial package of 5 pouch in 1 package / 30 g in 1 pouch of Derma Honey Mask, labeled by Cellalab. 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 Cellalab on March 01, 2018. The current certification is valid through December 31, 2019.

How is this Cellalab product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72312001001. 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)
72312-0010-1
11-Digit CMS (5-4-2)
72312-0010-01

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