Home NDC 68062-8312 Dr Lift Mineral SPF 30
Product NDC 68062-8312
11-digit product format 680628312
Labeler code 68062
Product ID 68062-8312_40c0e413-70f6-25c9-e063-6294a90ad27d
Type HUMAN OTC DRUG
Nonproprietary name titanium dioxide
Dosage form SPRAY
Route TOPICAL
Labeler Spa de Soleil
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-09
Substance TITANIUM DIOXIDE
Active strength 72 mg/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 Dr Lift Mineral SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 72 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 68062-8312-1 Dr Lift Mineral SPF 30 100 mL in 1 BOTTLE, SPRAY SPRAY 100 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 68062-8312-1 68062831201 100 mL in 1 BOTTLE, SPRAY (68062-8312-1) 100 ml 2025-10-09 No No Current