Phofay Matte Sunscreen Liquid Foundation Spf 30 6 Lotion
NDC Package 85161-129-01

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

Package Information

Phofay Matte Sunscreen Liquid Foundation Spf 30 6 (ensulizole , homosalate , octinoxate, titanium dioxide) lotions is helps prevent sunburnprovides high protection against sunburn and tanninglf used as directed with other sun protection measures.decreases the risk of skin cancer and early skin aging caused by the sun. This formulation utilizes a lotion delivery system. Marketed by Longway Technology(guangzhou) Co., Ltd., this product is identified by NDC 85161-129 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
85161-129-01
Package Description
1 BOTTLE in 1 BOX / 1 g in 1 BOTTLE
Product Code
11-Digit Billing Format
85161012901

Clinical Specifications

Proprietary Name
Phofay Matte Sunscreen Liquid Foundation Spf 30 6
Non-Proprietary Name
Ensulizole , Homosalate , Octinoxate, Titanium Dioxide
Substance Name
Ensulizole; Homosalate; Octinoxate; Titanium Dioxide
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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
Helps prevent sunburnprovides high protection against sunburn and tanninglf used as directed with other sun protection measures.decreases the risk of skin cancer and early skin aging caused by the sun

Regulatory & Marketing

Labeler Name
Longway Technology(guangzhou) Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-30-2025
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 85161-129-01 identifies a specific commercial package of 1 bottle in 1 box / 1 g in 1 bottle of Phofay Matte Sunscreen Liquid Foundation Spf 30 6, a human over the counter drug labeled by Longway Technology(guangzhou) Co., Ltd.. This lotion is formulated for topical use and contains ensulizole; homosalate; octinoxate; 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 Longway Technology(guangzhou) Co., Ltd. on August 30, 2025. The current certification is valid through December 31, 2026.

How is this Longway Technology(guangzhou) Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85161012901. 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)
85161-129-01
11-Digit CMS (5-4-2)
85161-0129-01

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