Sunscreen Stick
NDC Package 85473-444-50

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Sunscreen Stick sticks is a human otc drug administered via cutaneous route. This formulation utilizes a stick delivery system. Marketed by Guangzhou Yueyou Biological Technology Co., Ltd., this product is identified by NDC 85473-444 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
85473-444-50
Package Description
50 g in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
85473044450

Clinical Specifications

Proprietary Name
Sunscreen Stick
Non-Proprietary Name
Sunscreen Stick
Substance Name
Butyl Methoxydibenzoylmethane; Ethylhexyl Methoxycinnamate; Ethylhexyl Salicylate; Homosalate; Octocrylene; Titanium Dioxide
Dosage Form
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
Administration Route
Cutaneous - Administration to the skin.

Regulatory & Marketing

Labeler Name
Guangzhou Yueyou Biological Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2025
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 85473-444-50 identifies a specific commercial package of 50 g in 1 bottle, plastic of Sunscreen Stick, a human over the counter drug labeled by Guangzhou Yueyou Biological Technology Co., Ltd.. This stick is formulated for cutaneous use and contains butyl methoxydibenzoylmethane; ethylhexyl methoxycinnamate; ethylhexyl salicylate; homosalate; octocrylene; titanium dioxide 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 Yueyou Biological Technology Co., Ltd. on September 01, 2025. The current certification is valid through December 31, 2026.

How is this Guangzhou Yueyou Biological Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85473044450. 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)
85473-444-50
11-Digit CMS (5-4-2)
85473-0444-50

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