Home NDC 68577-289 IDEALOVE HYDROGLOW DAILY SUNSCREEN SPF 50
Product NDC 68577-289
11-digit product format 685770289
Labeler code 68577
Product ID 68577-289_564b28c0-42e9-be15-e063-6294a90a6a1e
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE
Dosage form CREAM
Route TOPICAL
Labeler COSMAX USA, CORP
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-01
Substance OCTISALATE; HOMOSALATE; AVOBENZONE
Active strength 5; 7.3; 3 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 IDEALOVE HYDROGLOW DAILY SUNSCREEN SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100mL HOMOSALATE 7.3 g/100mL AVOBENZONE 3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup V06SV4M95S Internal UNII lookup G63QQF2NOX Internal UNII lookup
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 68577-289-00 68577028900 1 TUBE in 1 CARTON (68577-289-00) / 100 mL in 1 TUBE 1 tube 2025-10-01 No No Current