Home NDC 69039-800 Sun Bum 50 Premium Moisturizing Sunscreen Roll-On
Product NDC 69039-800
11-digit product format 690390800
Labeler code 69039
Product ID 69039-800_3c58c9c7-ca9f-d012-e063-6394a90a5aa9
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler Sun Bum, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-01
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength 100; 50; 100; 30 mg/mL; mg/mL; 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 Premium Moisturizing Sunscreen Roll-On
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 100 mg/mL AVOBENZONE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 69039-800-01 Sun Bum 50 Premium Moisturizing Sunscreen Roll-On 88 mL in 1 TUBE, WITH APPLICATOR LOTION 88 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 69039-800-01 69039080001 88 mL in 1 TUBE, WITH APPLICATOR (69039-800-01) 88 ml 2025-01-01 No No Current