Sunscreen
NDC Package 83809-020-01

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 inactivated by the FDA.

Sunscreen is for sunscreen use: ● apply generously 15 minutes before sun exposure ● reapply: ● after 80 minutes of swimming or sweating ● immediately after towel drying ● at least every 2 hours ● Sun Protection Measures. Marketed by Shenzhen Yikai Electronic Technology Co., Ltd., this product is identified by NDC 83809-020 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
83809-020-01
Package Description
30 mL in 1 BOTTLE
Product Code
83809-020
11-Digit Billing Format
83809002001

Clinical Specifications

Proprietary Name
Sunscreen
Dosage Form
-
Usage Information
For sunscreen use: ● apply generously 15 minutes before sun exposure ● reapply: ● after 80 minutes of swimming or sweating ● immediately after towel drying ● at least every 2 hours ● Sun 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 value of 15 or higher and other sun protection measures including; ● limit time in the sun, especially from 10 am.-2 p.m. ● wear long-sleeved shirts, pants, hats and sunglasses ● children under 6 months of age: Ask a doctor

Regulatory & Marketing

Labeler Name
Shenzhen Yikai Electronic Technology Co., Ltd.
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-01-2024
Listing Expiration
12-31-2025
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (83809-020). Click a package code to view its specific billing and regulatory data.

83809-020-02
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 83809-020-01 identifies a specific commercial package of 30 ml in 1 bottle of Sunscreen, labeled by Shenzhen Yikai Electronic Technology 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 Shenzhen Yikai Electronic Technology Co., Ltd. on February 01, 2024. The current certification is valid through December 31, 2025.

How is this Shenzhen Yikai Electronic Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83809002001. 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)
83809-020-01
11-Digit CMS (5-4-2)
83809-0020-01

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