Home NDC 85772-0008 RYDEEN UV CLEAR
Product NDC 85772-0008
11-digit product format 857720008
Labeler code 85772
Product ID 85772-0008_54d2a9d1-b691-094a-e063-6394a90a98f6
Type HUMAN OTC DRUG
Nonproprietary name SUNSCREEN
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Oupeng Cosmetics Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-18
Substance PHENYLBENZIMIDAZOLE SULFONIC ACID; TITANIUM DIOXIDE; ETHYLHEXYL SALICYLATE; OCTOCRYLENE; HOMOSALATE
Active strength 3; 2.56; 3.9; 1.44; 3 g/100g; g/100g; 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 RYDEEN UV CLEAR
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENYLBENZIMIDAZOLE SULFONIC ACID 3 g/100g TITANIUM DIOXIDE 2.56 g/100g ETHYLHEXYL SALICYLATE 3.9 g/100g OCTOCRYLENE 1.44 g/100g HOMOSALATE 3 g/100g
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 27 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85772-0008-1 85772000801 1 BOTTLE in 1 BOX (85772-0008-1) / 40 g in 1 BOTTLE 1 bottle 2026-06-18 No No Current