Home NDC 87719-001 ANESSA PERFECT UV SUNSCREEN SKINCARE
Product NDC 87719-001
11-digit product format 877190001
Labeler code 87719
Product ID 87719-001_5347c9a1-223a-b617-e063-6294a90ac601
Type HUMAN OTC DRUG
Nonproprietary name Homosalate Octocrylene Ethylhexyl Salicylate
Dosage form SPRAY
Route TOPICAL
Labeler HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-01
Substance HOMOSALATE; OCTOCRYLENE; ETHYLHEXYL SALICYLATE
Active strength 8; 8; 4 g/100g; g/100g; g/100g
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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 8 g/100g OCTOCRYLENE 8 g/100g ETHYLHEXYL SALICYLATE 4 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 5A68WGF6WM Internal UNII lookup 4X49Y0596W 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 87719-001-01 87719000101 60 g in 1 BOTTLE (87719-001-01) 60 g 2026-06-01 No No Current