Sunscreen Setting Spritz, Spf 45 Spray
NDC Package 81522-228-01

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

Package Information

Sunscreen Setting Spritz, Spf 45 (sunscreen setting spray) sprays is directions Apply liberally 15 minutes before sun exposure. This formulation utilizes a spray delivery system. Marketed by Fsa Store Inc, this product is identified by NDC 81522-228 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
81522-228-01
Package Description
60 mL in 1 BOTTLE
Product Code
81522-228
11-Digit Billing Format
81522022801

Clinical Specifications

Proprietary Name
Sunscreen Setting Spritz, Spf 45
Non-Proprietary Name
Sunscreen Setting Spray
Substance Name
Avobenzone; Octisalate; Octocrylene
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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.
Active Ingredient(s)
Usage Information
Directions Apply liberally 15 minutes before sun exposure. Reaooly. at least every 2 hours or after 80 minutes ofswimming or sweating.Sun Protection Measures, Spending time in the sun increases your riskof skan cancer and early skin aging. lo decrease this risk, regularly use asunscreen with a Broad Spectrum SPF value of 15 or higher and other sunprotection measures including, limit time in sun, especiallv from 10 a.m.-2p.m, and wear long-sleeved shirts, pants, hats, and sunalasses. Chitdrenunder 6 months of age: ask a doctor.

Regulatory & Marketing

Labeler Name
Fsa Store Inc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-30-2025
Listing Expiration
12-31-2026
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 81522-228-01 identifies a specific commercial package of 60 ml in 1 bottle of Sunscreen Setting Spritz, Spf 45, a human over the counter drug labeled by Fsa Store Inc. This spray is formulated for topical use and contains avobenzone; octisalate; octocrylene 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 Fsa Store Inc on December 30, 2025. The current certification is valid through December 31, 2026.

How is this Fsa Store Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81522022801. 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)
81522-228-01
11-Digit CMS (5-4-2)
81522-0228-01

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