Juyasuyon Sport Ultra Sunscreen Spray
NDC Package 83566-622-01

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

Package Information

Juyasuyon Sport Ultra Sunscreen (avobenzone, homosalate, octisalate, octocrylene) sprays is shake well. This formulation utilizes a spray delivery system. Marketed by Guangdong Aimu Biological Technology Co., Ltd, this product is identified by NDC 83566-622 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
83566-622-01
Package Description
150 mL in 1 BOTTLE, SPRAY
Product Code
83566-622
11-Digit Billing Format
83566062201

Clinical Specifications

Proprietary Name
Juyasuyon Sport Ultra Sunscreen
Non-Proprietary Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
Shake well. Hold container 4 to 6 inches from the skin to apply. Spray liberally and spread evenly by hand 15 minutes before sun exposure. Do not apply directly into face. Spray on hands then apply to face. Do not use on windy days. Use in well-ventilated area. Reapply: • after 80 minutes of swimming or sweating • immediately after towel dry • reapply at least every 2 hours • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months of age: Ask a doctor.

Regulatory & Marketing

Labeler Name
Guangdong Aimu Biological Technology Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-25-2026
Listing Expiration
12-31-2027
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 83566-622-01 identifies a specific commercial package of 150 ml in 1 bottle, spray of Juyasuyon Sport Ultra Sunscreen, a human over the counter drug labeled by Guangdong Aimu Biological Technology Co., Ltd. This spray is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 Guangdong Aimu Biological Technology Co., Ltd on August 25, 2026. The current certification is valid through December 31, 2027.

How is this Guangdong Aimu Biological Technology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83566062201. 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)
83566-622-01
11-Digit CMS (5-4-2)
83566-0622-01

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