Home NDC 59088-568 DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen
Product NDC 59088-568
11-digit product format 590880568
Labeler code 59088
Product ID 59088-568_23848119-f005-7528-e063-6394a90a9a0e
Type HUMAN OTC DRUG
Nonproprietary name avobenzone, octinoxate, octisalate, titanium dioxide
Dosage form LOTION
Route TOPICAL
Labeler PureTek Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-02-16
Substance AVOBENZONE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
Active strength 25; 30; 30; 12.5 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 DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 25 mg/mL OCTINOXATE 30 mg/mL OCTISALATE 30 mg/mL TITANIUM DIOXIDE 12.5 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59088-568-05 DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen 56 mL in 1 BOTTLE LOTION 56 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59088-568 DERMACINRX SKIN MOISTURIZING ULTRA SPF 50 SUNSCREEN (AVOBENZONE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE) LOTION [PURETEK CORPORATION] 5 Current NDC, Legacy NDC, 1 package rows 20241004_86eb06cc-d63f-4500-a52e-14ef99a56532.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 Marketing end Sample Exclude flag Status 59088-568-05 59088056805 56 mL in 1 BOTTLE (59088-568-05) 56 ml 2017-02-16 0000-00-00 No No Current