Sunscreenspray
NDC Package 84423-090-01

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

Package Information

Sunscreenspray (sunscreen spray) sprays is very high, broad spectrum protection for the body against UVA and UVB. This formulation utilizes a spray delivery system. Marketed by Guangzhou Kadiya Biotechnology Co., Ltd., this product is identified by NDC 84423-090 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
84423-090-01
Package Description
100 g in 1 BOTTLE, SPRAY
Product Code
84423-090
11-Digit Billing Format
84423009001

Clinical Specifications

Proprietary Name
Sunscreenspray
Non-Proprietary Name
Sunscreen Spray
Substance Name
Niacinamide; Zinc Oxide
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
Very high, broad spectrum protection for the body against UVA and UVB. Suitable for all skin types, especially those with very clear, sensitive phototypes and sun intolerance.

Regulatory & Marketing

Labeler Name
Guangzhou Kadiya Biotechnology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-04-2025
Listing Expiration
12-31-2026
Exclude Flag
N
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 84423-090-01 identifies a specific commercial package of 100 g in 1 bottle, spray of Sunscreenspray, a human over the counter drug labeled by Guangzhou Kadiya Biotechnology Co., Ltd.. This spray is formulated for cutaneous use and contains niacinamide; zinc oxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Guangzhou Kadiya Biotechnology Co., Ltd. on August 04, 2025. The current certification is valid through December 31, 2026.

How is this Guangzhou Kadiya Biotechnology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84423009001. 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)
84423-090-01
11-Digit CMS (5-4-2)
84423-0090-01

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