Home NDC 70707-455 Face Reality Brilliant Defense Sunscreen SPF 50
Product NDC 70707-455
11-digit product format 707070455
Labeler code 70707
Product ID 70707-455_3b16f4e6-63a7-9249-e063-6394a90a4461
Type HUMAN OTC DRUG
Nonproprietary name OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE
Dosage form CREAM
Route TOPICAL
Labeler Face Reality,�LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-15
Substance OCTOCRYLENE; HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength 90; 60; 50; 30 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Face Reality Brilliant Defense Sunscreen SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 90 mg/mL HOMOSALATE 60 mg/mL OCTISALATE 50 mg/mL AVOBENZONE 30 mg/mL
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70707-455-01 Face Reality Brilliant Defense Sunscreen SPF 50 60 mL in 1 TUBE CREAM 60 1
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 70707-455-01 70707045501 60 mL in 1 TUBE (70707-455-01) 60 ml 2025-11-15 No No Current