Home NDC 75376-697 Sport Ultra
Product NDC 75376-697
11-digit product format 753760697
Labeler code 75376
Product ID 75376-697_5268de76-6f9f-40d7-e063-6394a90ae3a1
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler Guangzhou Danting Bath&Body Care Industry Co. Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-17
Substance OCTISALATE; OCTOCRYLENE; AVOBENZONE; HOMOSALATE
Active strength 4.5; 6.5; 2.7; 9 g/100mL; g/100mL; g/100mL; g/100mL
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 Sport Ultra
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 4.5 g/100mL OCTOCRYLENE 6.5 g/100mL AVOBENZONE 2.7 g/100mL HOMOSALATE 9 g/100mL
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 75376-697-08 Sport Ultra 236 mL in 1 BOTTLE LOTION 236 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 75376-697-08 75376069708 236 mL in 1 BOTTLE (75376-697-08) 236 ml 2025-06-17 No No Current