Guinot Ultra Uv Sunscreen High Protection Sun Cream For The Face And Body Spf 30
NDC Package 54181-003-50

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 discontinued by the firm.

Guinot Ultra Uv Sunscreen High Protection Sun Cream For The Face And Body Spf 30 is a . Marketed by Guinot Sas, this product is identified by NDC 54181-003 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
54181-003-50
Package Description
1 TUBE in 1 PACKAGE / 50 mL in 1 TUBE
Product Code
54181-003
11-Digit Billing Format
54181000350

Clinical Specifications

Proprietary Name
Guinot Ultra Uv Sunscreen High Protection Sun Cream For The Face And Body Spf 30
Dosage Form
-

Regulatory & Marketing

Labeler Name
Guinot Sas
FDA Application #
part352
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
01-02-2014
End Marketing Date
01-01-2018
Listing Expiration
01-01-2018
Exclude Flag
D
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 54181-003-50 identifies a specific commercial package of 1 tube in 1 package / 50 ml in 1 tube of Guinot Ultra Uv Sunscreen High Protection Sun Cream For The Face And Body Spf 30, labeled by Guinot Sas. 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 Guinot Sas on January 02, 2014. The current certification is valid through January 01, 2018.

How is this Guinot Sas product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54181000350. 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)
54181-003-50
11-Digit CMS (5-4-2)
54181-0003-50

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