Home NDC 83810-012 Broad Spectrum SPF 50 sunscreen
Product NDC 83810-012
11-digit product format 838100012
Labeler code 83810
Product ID 83810-012_3d4ad2e7-1697-0ca3-e063-6394a90ab97e
Type HUMAN OTC DRUG
Nonproprietary name Homosalate 10%, Octisalate 5.0%, Avobenzone 3.0%
Dosage form SPRAY
Route TOPICAL
Labeler Florida Squeezed
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-25
Substance AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength 3; 15; 10 g/100g; g/100g; g/100g
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 Broad Spectrum SPF 50 sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100g HOMOSALATE 15 g/100g OCTISALATE 10 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W 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 83810-012-06 Broad Spectrum SPF 50 sunscreen 170 g in 1 CAN SPRAY 170 2
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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83810-012-06 83810001206 170 g in 1 CAN (83810-012-06) 170 g 2025-08-26 No No Current