Ganrek Sunscreen Sprayer Broad Spectrum Spf 50 Aerosol, Spray
NDC Package 84167-424-03

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

Package Information

Ganrek Sunscreen Sprayer Broad Spectrum Spf 50 (sunscreen spf 50) aerosols is directions for Use: For sunscreen useShake well before use.Hold the spray 15-20 cm away from theskin and apply evenly.Do not spray directly onto the face.For facial application, spray onto thepalms or a cotton pad first, then gentlypat onto the face. This formulation utilizes a aerosol, spray delivery system. Marketed by Guangzhou Meixi Biotechnology Co., Ltd., this product is identified by NDC 84167-424 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
84167-424-03
Package Description
1 BOTTLE, SPRAY in 1 BOTTLE, SPRAY / 1 AEROSOL, SPRAY in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
84167042403

Clinical Specifications

Proprietary Name
Ganrek Sunscreen Sprayer Broad Spectrum Spf 50
Non-Proprietary Name
Sunscreen Spf 50
Substance Name
Avobenzone; Homosalate; Octisalate
Dosage Form
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
Administration Route
Extracorporeal - Administration outside of the body.
Usage Information
Directions for Use: For sunscreen useShake well before use.Hold the spray 15-20 cm away from theskin and apply evenly.Do not spray directly onto the face.For facial application, spray onto thepalms or a cotton pad first, then gentlypat onto the face.

Regulatory & Marketing

Labeler Name
Guangzhou Meixi Biotechnology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-07-2026
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 84167-424-03 identifies a specific commercial package of 1 bottle, spray in 1 bottle, spray / 1 aerosol, spray in 1 bottle, spray of Ganrek Sunscreen Sprayer Broad Spectrum Spf 50, a human over the counter drug labeled by Guangzhou Meixi Biotechnology Co., Ltd.. This aerosol, spray is formulated for extracorporeal use and contains avobenzone; homosalate; octisalate 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 Meixi Biotechnology Co., Ltd. on February 07, 2026. The current certification is valid through December 31, 2027.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84167042403. 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)
84167-424-03
11-Digit CMS (5-4-2)
84167-0424-03

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