Home NDC 69039-672 Sun Bum 30 Premium Moisturizing Sunscreen
Product NDC 69039-672
11-digit product format 690390672
Labeler code 69039
Product ID 69039-672_3ce694ab-5a5c-7885-e063-6394a90a0a73
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 2024-06-01
Substance HOMOSALATE; AVOBENZONE; OCTOCRYLENE; OCTISALATE
Active strength 50; 30; 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 30 Premium Moisturizing Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 50 mg/mL AVOBENZONE 30 mg/mL OCTOCRYLENE 100 mg/mL OCTISALATE 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 69039-672-00 Sun Bum 30 Premium Moisturizing Sunscreen 473 mL in 1 BOTTLE, PUMP LOTION 473 4
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 238 of 346 · 6,912 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69039-672-00 69039067200 473 mL in 1 BOTTLE, PUMP (69039-672-00) 473 ml 2024-06-01 No No Current