Seranovatm Ultralight Spf50 Serum Cream
NDC Package 84148-022-01

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

Package Information

Seranovatm Ultralight Spf50 Serum cream is - Shake well before use. This formulation utilizes a cream delivery system. Marketed by Guangzhou Ariel Biotech Co., Ltd., this product is identified by NDC 84148-022 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
84148-022-01
Package Description
50 mL in 1 BOTTLE
Product Code
84148-022
11-Digit Billing Format
84148002201

Clinical Specifications

Proprietary Name
Seranovatm Ultralight Spf50 Serum
Non-Proprietary Name
Seranovatm Ultralight Spf50 Serum
Substance Name
Butyl Methoxydibenzoylmethane; Ethylhexyl Methoxycinnamate; Ethylhexyl Salicylate; Titanium Dioxide
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
- Shake well before use. Apply to face liberally and evenly 15 minutes before sun exposure. - Reapply every 2 hours.use a water- resistant sunscreen if swimming or sweating. - For use on children less than 6 months of age consult a doctor.

Regulatory & Marketing

Labeler Name
Guangzhou Ariel Biotech Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2026
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 84148-022-01 identifies a specific commercial package of 50 ml in 1 bottle of Seranovatm Ultralight Spf50 Serum, a human over the counter drug labeled by Guangzhou Ariel Biotech Co., Ltd.. This cream is formulated for cutaneous use and contains butyl methoxydibenzoylmethane; ethylhexyl methoxycinnamate; 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 Guangzhou Ariel Biotech Co., Ltd. on April 01, 2026. The current certification is valid through December 31, 2027.

How is this Guangzhou Ariel Biotech Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84148002201. 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)
84148-022-01
11-Digit CMS (5-4-2)
84148-0022-01

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