Home NDC 87283-004 ALOHA MINERAL BLOCK-BRUSH ON MINERAL
Product NDC 87283-004
11-digit product format 872830004
Labeler code 87283
Product ID 87283-004_47dd07aa-71b5-5d54-e063-6394a90a4127
Type HUMAN OTC DRUG
Nonproprietary name SUNSCREEN SPF50
Dosage form POWDER
Route TOPICAL
Labeler Aopline Biotechnology (Guangzhou) Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-08
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 19.5; 24 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 ALOHA MINERAL BLOCK-BRUSH ON MINERAL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 19.5 g/100g ZINC OXIDE 24 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z 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 87283-004-01 ALOHA MINERAL BLOCK-BRUSH ON MINERAL 6 g in 1 BOTTLE POWDER 6 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 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 87283-004-01 87283000401 6 g in 1 BOTTLE (87283-004-01) 6 g 2026-01-08 No No Current