Home NDC 87719-002 ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB
Product NDC 87719-002
11-digit product format 877190002
Labeler code 87719
Product ID 87719-002_5354af18-50c5-5fba-e063-6394a90ace39
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide Octocrylene Ethylhexyl Salicylate Homosalate Titanium Dioxide
Dosage form LOTION
Route TOPICAL
Labeler HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-03
Substance HOMOSALATE; ZINC OXIDE; TITANIUM DIOXIDE; OCTOCRYLENE; ETHYLHEXYL SALICYLATE
Active strength 8; 10; 3; 8; 4 g/100mL; 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 ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 8 g/100mL ZINC OXIDE 10 g/100mL TITANIUM DIOXIDE 3 g/100mL OCTOCRYLENE 8 g/100mL ETHYLHEXYL SALICYLATE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 87719-002-01 87719000201 60 mL in 1 BOTTLE (87719-002-01) 60 ml 2026-06-03 No No Current