Home NDC 70707-453 Face Reality daily spf 30 plus Sunscreen SPF 30
Product NDC 70707-453
11-digit product format 707070453
Labeler code 70707
Product ID 70707-453_29b6b0a2-bf12-1241-e063-6394a90a169e
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, AVOBENZONE
Dosage form CREAM
Route TOPICAL
Labeler Face Reality,�LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-17
Substance HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength 100; 50; 30 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 daily spf 30 plus Sunscreen SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL AVOBENZONE 30 mg/mL
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 4X49Y0596W Internal UNII lookup G63QQF2NOX Internal UNII lookup
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 70707-453-01 Face Reality daily spf 30 plus Sunscreen SPF 30 1 in 1 CARTON CREAM 1 1 70707-453-01 Face Reality daily spf 30 plus Sunscreen SPF 30 60 mL in 1 TUBE CREAM 60 1 70707-453-02 Face Reality daily spf 30 plus Sunscreen SPF 30 1 in 1 CARTON CREAM 1 1 70707-453-02 Face Reality daily spf 30 plus Sunscreen SPF 30 118 mL in 1 TUBE CREAM 118 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70707-453 FACE REALITY DAILY SPF 30 PLUS SUNSCREEN SPF 30 (HOMOSALATE, OCTISALATE, AVOBENZONE) CREAM [FACE REALITY, LLC] 1 Current NDC, 4 package rows 20250117_45a3ce12-15fe-4040-95da-ac8513a39fb9.zip
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 70707-453-01 70707045301 1 TUBE in 1 CARTON (70707-453-01) / 60 mL in 1 TUBE 1 tube 2025-01-17 No No Current 70707-453-02 70707045302 1 TUBE in 1 CARTON (70707-453-02) / 118 mL in 1 TUBE 1 tube 2025-01-17 No No Current