Home NDC 84090-003 PURE SOL SPF 30 Mineral Whipped Sunscreen
Product NDC 84090-003
11-digit product format 840900003
Labeler code 84090
Product ID 84090-003_4051e1fb-855e-76fa-e063-6394a90ac5e7
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form SPRAY
Route TOPICAL
Labeler Brand 2022b LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-04
Substance ZINC OXIDE
Active strength 15 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 PURE SOL SPF 30 Mineral Whipped Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 15 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 84090-003-01 PURE SOL SPF 30 Mineral Whipped Sunscreen 166 mL in 1 BOTTLE SPRAY 166 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 84090-003-01 84090000301 166 mL in 1 BOTTLE (84090-003-01) 166 ml 2025-10-04 No No Current