Sunscreen Lotion
NDC Package 87357-001-01

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

Package Information

Sunscreen (titanium dioxide) lotions is helps prevent sunburn If used as directed with other sun protection measures(see Directions),decreases the risk of skin cancer and early skin aging caused by the sun. This formulation utilizes a lotion delivery system. Marketed by Guangdong Zhoubang Biotechnology Co., Ltd, this product is identified by NDC 87357-001 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
87357-001-01
Package Description
30 mL in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
87357000101

Clinical Specifications

Proprietary Name
Sunscreen
Non-Proprietary Name
Titanium Dioxide
Substance Name
Ethylhexyl Salicylate; Titanium Dioxide
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route
Cutaneous - Administration to the skin.
Usage Information
Helps prevent sunburn If used as directed with other sun protection measures(see Directions),decreases the risk of skin cancer and early skin aging caused by the sun.

Regulatory & Marketing

Labeler Name
Guangdong Zhoubang Biotechnology Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-22-2026
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 87357-001-01 identifies a specific commercial package of 30 ml in 1 bottle, glass of Sunscreen, a human over the counter drug labeled by Guangdong Zhoubang Biotechnology Co., Ltd. This lotion is formulated for cutaneous use and contains ethylhexyl salicylate; 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 Guangdong Zhoubang Biotechnology Co., Ltd on January 22, 2026. The current certification is valid through December 31, 2027.

How is this Guangdong Zhoubang Biotechnology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87357000101. 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)
87357-001-01
11-Digit CMS (5-4-2)
87357-0001-01

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