Home NDC 87552-001 uLOOK Sunscreen SPF 50
Product NDC 87552-001
11-digit product format 875520001
Labeler code 87552
Product ID 87552-001_4f0e5189-d94e-a556-e063-6394a90a7a07
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form CREAM
Route TOPICAL
Labeler HAMEX GLOBAL COSMETICS LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-27
Substance OCTINOXATE; OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE; TITANIUM DIOXIDE
Active strength 72.8; 30.8; 64.4; 84; 28; 20 mg/g; mg/g; mg/g; mg/g; mg/g; mg/g
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 uLOOK Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 72.8 mg/g OCTISALATE 30.8 mg/g HOMOSALATE 64.4 mg/g OCTOCRYLENE 84 mg/g AVOBENZONE 28 mg/g TITANIUM DIOXIDE 20 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87552-001-01 uLOOK Sunscreen SPF 50 50 g in 1 BOTTLE, PUMP CREAM 50 2
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 87552-001-01 87552000101 50 g in 1 BOTTLE, PUMP (87552-001-01) 50 g 2026-03-29 No No Current