Home NDC 84484-001 100% MINERAL SUNSCREEN
Product NDC 84484-001
11-digit product format 844840001
Labeler code 84484
Product ID 84484-001_3c4a3b4a-ac90-8ce7-e063-6294a90abe18
Type HUMAN OTC DRUG
Nonproprietary name 100% MINERAL SUNSCREEN
Dosage form CREAM
Route CUTANEOUS
Labeler Guangzhou Pallas Cosmetics Co.,Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-14
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 15; 10 g/100mL; g/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 100% MINERAL SUNSCREEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 15 g/100mL TITANIUM DIOXIDE 10 g/100mL
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 84484-001-01 100% MINERAL SUNSCREEN 50 mL in 1 BOTTLE CREAM 50 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 84484-001-01 84484000101 50 mL in 1 BOTTLE (84484-001-01) 50 ml 2025-08-14 No No Current