Home NDC 69039-734 Sun Bum 30 Mineral Tinted Sunscreen Face
Product NDC 69039-734
11-digit product format 690390734
Labeler code 69039
Product ID 69039-734_3d623fe7-f1f9-a67e-e063-6294a90af9a9
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Sun Bum, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-01
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 24; 58 mg/mL; mg/mL
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 Sun Bum 30 Mineral Tinted Sunscreen Face
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 24 mg/mL TITANIUM DIOXIDE 58 mg/mL
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 69039-734-01 Sun Bum 30 Mineral Tinted Sunscreen Face 50 mL in 1 TUBE LOTION 50 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 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 69039-734-01 69039073401 50 mL in 1 TUBE (69039-734-01) 50 ml 2025-01-01 No No Current