Home NDC 53675-213 Aruba Aloe Hand Sanitizer
Product NDC 53675-213
11-digit product format 536750213
Labeler code 53675
Product ID 53675-213_3bc6d7a9-3a5b-92eb-e063-6294a90a5a37
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form CREAM
Route TOPICAL
Labeler Aruba Aloe Balm NV
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-15
Substance ALCOHOL
Active strength 80 mL/100mL
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 Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 80 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M 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 53675-213-00 Aruba Aloe Hand Sanitizer 59 mL in 1 TUBE CREAM 59 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 53675-213-00 53675021300 59 mL in 1 TUBE (53675-213-00) 59 ml 2025-06-15 No No Current