Shiseido White Lucent Brightening Spot-control Foundation (refill)
NDC Package 52686-252-30

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.

Shiseido White Lucent Brightening Spot-control Foundation (refill) is for sunscreen use:apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hoursSun Protection Measures. Marketed by Shiseido America Inc., this product is identified by NDC 52686-252 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
52686-252-30
Package Description
1 TRAY in 1 CARTON / 10 g in 1 TRAY
Product Code
52686-252
11-Digit Billing Format
52686025230

Clinical Specifications

Proprietary Name
Shiseido White Lucent Brightening Spot-control Foundation (refill) O00
Dosage Form
-
Usage Information
For sunscreen use:apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hoursSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. – 2 p.m.wear long-sleeve shirts, pants, hats, and sunglasseschildren under 6 months: Ask a doctor

Regulatory & Marketing

Labeler Name
Shiseido America Inc.
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
03-01-2011
End Marketing Date
12-01-2015
Listing Expiration
12-01-2015
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 52686-252-30 identifies a specific commercial package of 1 tray in 1 carton / 10 g in 1 tray of Shiseido White Lucent Brightening Spot-control Foundation (refill) O00, labeled by Shiseido America 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 Shiseido America Inc. on March 01, 2011. The current certification is valid through December 01, 2015.

How is this Shiseido America Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52686025230. 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)
52686-252-30
11-Digit CMS (5-4-2)
52686-0252-30

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