Home NDC 69039-735 Sun Bum 50 Mineral Sunscreen Roll-On
Product NDC 69039-735
11-digit product format 690390735
Labeler code 69039
Product ID 69039-735_3c5c6c32-5fe1-03e3-e063-6294a90a3679
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 TITANIUM DIOXIDE; ZINC OXIDE
Active strength 34; 160 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 50 Mineral Sunscreen Roll-On
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 34 mg/mL ZINC OXIDE 160 mg/mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69039-735-01 Sun Bum 50 Mineral Sunscreen Roll-On 88 mL in 1 TUBE, WITH APPLICATOR LOTION 88 2
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 45 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 69039-735-01 69039073501 88 mL in 1 TUBE, WITH APPLICATOR (69039-735-01) 88 ml 2025-01-01 No No Current