Fenty Skin Hydra Vizor
NDC Package 71499-101-12

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Fenty Skin Hydra Vizor is a . Marketed by Kendo Holdings Inc, this product is identified by NDC 71499-101 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
71499-101-12
Package Description
30 mL in 1 TUBE
Product Code
71499-101
11-Digit Billing Format
71499010112

Clinical Specifications

Proprietary Name
Fenty Skin Hydra Vizor Spf 30
Dosage Form
-

Regulatory & Marketing

Labeler Name
Kendo Holdings Inc
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-23-2020
End Marketing Date
08-23-2020
Listing Expiration
08-23-2020
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71499-101). Click a package code to view its specific billing and regulatory data.

71499-101-11
7 mL in 1 TUBE
71499-101-13
50 mL in 1 BOTTLE

* 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 71499-101-12 identifies a specific commercial package of 30 ml in 1 tube of Fenty Skin Hydra Vizor Spf 30, labeled by Kendo Holdings Inc. 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 Kendo Holdings Inc on August 23, 2020. The current certification is valid through August 23, 2020.

How is this Kendo Holdings Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71499010112. 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)
71499-101-12
11-Digit CMS (5-4-2)
71499-0101-12

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