Home NDC 87593-101 MENS SPF50 ALL IN ONE SUNSCREEN
Product NDC 87593-101
11-digit product format 875930101
Labeler code 87593
Product ID 87593-101_57074480-77fe-cc06-e063-6294a90a28d4
Type HUMAN OTC DRUG
Nonproprietary name MENS SPF50 ALL IN ONE SUNSCREEN
Dosage form CREAM
Route CUTANEOUS
Labeler Lance (Guangzhou) Biological Technology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-20
Substance HOMOSALATE; OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE
Active strength 4.9; 2.5; 6; 2 g/50g; g/50g; g/50g; g/50g
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 MENS SPF50 ALL IN ONE SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 4.9 g/50g OCTISALATE 2.5 g/50g ZINC OXIDE 6 g/50g TITANIUM DIOXIDE 2 g/50g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 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 87593-101-50 87593010150 50 g in 1 TUBE (87593-101-50) 50 g 2026-07-20 No No Current