Home NDC 69039-663 Sun Bum Daily Body
Product NDC 69039-663
11-digit product format 690390663
Labeler code 69039
Product ID 69039-663_3f7f1343-719a-8676-e063-6394a90a4cda
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 2024-02-26
Substance OCTISALATE; AVOBENZONE; OCTOCRYLENE; HOMOSALATE
Active strength 50; 30; 90; 80 mg/mL; mg/mL; mg/mL; mg/mL
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 Sun Bum Daily Body
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 50 mg/mL AVOBENZONE 30 mg/mL OCTOCRYLENE 90 mg/mL HOMOSALATE 80 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 69039-663-01 Sun Bum Daily Body 237 mL in 1 BOTTLE, PLASTIC LOTION 237 5
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 69039-663-01 69039066301 237 mL in 1 BOTTLE, PLASTIC (69039-663-01) 237 ml 2024-02-26 No No Current