Home NDC 81100-508 ISNTREE HYALURONIC ACID WATERY SUNSCREEN
Product NDC 81100-508
11-digit product format 811000508
Labeler code 81100
Product ID 81100-508_59e9279a-2429-d6bc-e063-6394a90ae86e
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler ISNTREE Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-30
Substance OCTISALATE; OCTOCRYLENE; HOMOSALATE; AVOBENZONE
Active strength 2.25; 4.5; 3.5; 1.425 g/50mL; g/50mL; g/50mL; g/50mL
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 ISNTREE HYALURONIC ACID WATERY SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 2.25 g/50mL OCTOCRYLENE 4.5 g/50mL HOMOSALATE 3.5 g/50mL AVOBENZONE 1.425 g/50mL
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.
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 81100-508-02 81100050802 1 TUBE in 1 BOX (81100-508-02) / 50 mL in 1 TUBE (81100-508-01) 1 tube 2026-06-30 No No Current