Oceaura Glitter Sunscreen Liquid
NDC Package 85064-020-01

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

Package Information

Oceaura Glitter Sunscreen (titanium dioxide) liquids is 1. This formulation utilizes a liquid delivery system. Marketed by Guangzhou Oceaura Biotechnology Co., Ltd., this product is identified by NDC 85064-020 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
85064-020-01
Package Description
50 mg in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
85064002001

Clinical Specifications

Proprietary Name
Oceaura Glitter Sunscreen
Non-Proprietary Name
Titanium Dioxide
Substance Name
Hibiscus Sabdariffa Seed Oil; Persea Gratissima (avocado) Oil
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Usage Information
1. Shake well before use.2. Spray evenly on face or body while keeping a distance.3. Wait for absorption.

Regulatory & Marketing

Labeler Name
Guangzhou Oceaura Biotechnology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-29-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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 85064-020-01 identifies a specific commercial package of 50 mg in 1 bottle, glass of Oceaura Glitter Sunscreen, a human over the counter drug labeled by Guangzhou Oceaura Biotechnology Co., Ltd.. This liquid is formulated for topical use and contains hibiscus sabdariffa seed oil; persea gratissima (avocado) oil 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 Oceaura Biotechnology Co., Ltd. on November 29, 2025. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85064002001. 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)
85064-020-01
11-Digit CMS (5-4-2)
85064-0020-01

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