Home NDC 81522-228 Sunscreen Setting Spritz, SPF 45
Product NDC 81522-228
11-digit product format 815220228
Labeler code 81522
Product ID 81522-228_473d6804-8d21-6899-e063-6294a90a3131
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen setting spray
Dosage form SPRAY
Route TOPICAL
Labeler FSA Store Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-30
Substance OCTISALATE; AVOBENZONE; OCTOCRYLENE
Active strength 2.94; 1.74; 5.7 g/60mL; g/60mL; g/60mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Sunscreen Setting Spritz, SPF 45
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 2.94 g/60mL AVOBENZONE 1.74 g/60mL OCTOCRYLENE 5.7 g/60mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup G63QQF2NOX Internal UNII lookup 5A68WGF6WM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81522-228-01 Sunscreen Setting Spritz, SPF 45 60 mL in 1 BOTTLE SPRAY 60 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 242 of 353 · 7,041 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81522-228-01 81522022801 60 mL in 1 BOTTLE (81522-228-01) 60 ml 2025-12-30 No No Current