Esopinio Sun Shield Plus
NDC Package 44781-110-01

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.

Esopinio Sun Shield Plus is indications and Usage:Tighten the lid after using it.Don't keep it in the place where the temperature is extremely hot or low and exposed the direct sunlight.Please apply it an adequate quantity  evenly on face, throat, arms and legs at the last stage of basic makeup.Please apply it once again on your skin at the time when you're going out, sports activity, and any activities of outside. Marketed by Zion Synthetic Fiber Co., Ltd., this product is identified by NDC 44781-110 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
44781-110-01
Package Description
70 mL in 1 CARTON
Product Code
44781-110
11-Digit Billing Format
44781011001

Clinical Specifications

Proprietary Name
Esopinio Sun Shield Plus Spf 35 Pa
Dosage Form
-
Usage Information
Indications and Usage:Tighten the lid after using it.Don't keep it in the place where the temperature is extremely hot or low and exposed the direct sunlight.Please apply it an adequate quantity  evenly on face, throat, arms and legs at the last stage of basic makeup.Please apply it once again on your skin at the time when you're going out, sports activity, and any activities of outside.

Regulatory & Marketing

Labeler Name
Zion Synthetic Fiber Co., Ltd.
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-01-2010
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 44781-110-01 identifies a specific commercial package of 70 ml in 1 carton of Esopinio Sun Shield Plus Spf 35 Pa, labeled by Zion Synthetic Fiber 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 Zion Synthetic Fiber Co., Ltd. on April 01, 2010. The current certification is valid through December 31, 2017.

How is this Zion Synthetic Fiber Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44781011001. 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)
44781-110-01
11-Digit CMS (5-4-2)
44781-0110-01

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