Home NDC 61477-232-01 Aloe Up SPF 50 Mineral
Product NDC 61477-232
Requested package NDC 61477-232-01
11-digit product format 614770232
Labeler code 61477
Product ID 61477-232_37d95f06-6460-88da-e063-6394a90a6dcd
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form SPRAY
Route TOPICAL
Labeler Aloe Care International, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-22
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 19.5; 4 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 Aloe Up SPF 50 Mineral
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 19.5 g/100g TITANIUM DIOXIDE 4 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP 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 61477-232-01 Aloe Up SPF 50 Mineral 128 g in 1 CAN SPRAY 128 3
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 111 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 61477-232-01 61477023201 128 g in 1 CAN (61477-232-01) 128 g 2025-05-22 No No Current