Home NDC 52260-018 Sunscreen SPF 50
Product NDC 52260-018
11-digit product format 522600018
Labeler code 52260
Product ID 52260-018_55f372a8-6bb2-b36a-e063-6294a90a89dc
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone 3% Homosalate 10% Octocrylene 5%
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Worthy Promotional Products
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-02
Substance AVOBENZONE; HOMOSALATE; OCTOCRYLENE
Active strength 3; 10; 5 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100g HOMOSALATE 10 g/100g OCTOCRYLENE 5 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 5A68WGF6WM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 52260-018-06 52260001806 156 g in 1 CAN (52260-018-06) 156 g 2026-03-02 No No Current