Isleaf Energy Water
NDC Package 70818-014-01

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.

Isleaf Energy Water is apply fair amount of Energy Water Cream onto all parts of the face and neck avoiding the eye contour area at the last step of the skin care. Marketed by C3 Co., Ltd., this product is identified by NDC 70818-014 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
70818-014-01
Package Description
100 g in 1 TUBE
Product Code
70818-014
11-Digit Billing Format
70818001401

Clinical Specifications

Proprietary Name
Isleaf Energy Water
Dosage Form
-
Usage Information
Apply fair amount of Energy Water Cream onto all parts of the face and neck avoiding the eye contour area at the last step of the skin care

Regulatory & Marketing

Labeler Name
C3 Co., Ltd.
FDA Application #
part347
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
08-08-2017
Listing Expiration
12-31-2021
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 70818-014-01 identifies a specific commercial package of 100 g in 1 tube of Isleaf Energy Water, labeled by C3 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 C3 Co., Ltd. on August 08, 2017. The current certification is valid through December 31, 2021.

How is this C3 Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70818001401. 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)
70818-014-01
11-Digit CMS (5-4-2)
70818-0014-01

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