Home NDC 53675-214 Aruba Aloe Hydrating Aloe Rich Sunscreen SPF 15
Product NDC 53675-214
11-digit product format 536750214
Labeler code 53675
Product ID 53675-214_3c3fb566-c899-287f-e063-6394a90ace96
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
Dosage form CREAM
Route TOPICAL
Labeler Aruba Aloe Balm NV
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-31
Substance AVOBENZONE; HOMOSALATE; OCTOCRYLENE; OCTISALATE
Active strength 30; 73.4; 50; 50 mg/mL; mg/mL; mg/mL; mg/mL
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 Aruba Aloe Hydrating Aloe Rich Sunscreen SPF 15
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 73.4 mg/mL OCTOCRYLENE 50 mg/mL OCTISALATE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 53675-214-00 Aruba Aloe Hydrating Aloe Rich Sunscreen SPF 15 177 mL in 1 TUBE CREAM 177 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 26 of 361 · 7,213 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 53675-214-00 53675021400 177 mL in 1 TUBE (53675-214-00) 177 ml 2025-05-31 No No Current