Home NDC 71501-1902 Urban Antioxidant Sunscreen SPF 40
Product NDC 71501-1902
11-digit product format 715011902
Labeler code 71501
Product ID 71501-1902_32d451f8-c8a1-7433-e063-6394a90a71c3
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Octocrylene, Zinc Oxyide cream
Dosage form CREAM
Route TOPICAL
Labeler Dr. Loretta, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-09-16
Substance HOMOSALATE; OCTOCRYLENE; ZINC OXIDE; OCTISALATE
Active strength 80; 50; 80; 50 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 Urban Antioxidant Sunscreen SPF 40
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 80 mg/mL OCTOCRYLENE 50 mg/mL ZINC OXIDE 80 mg/mL OCTISALATE 50 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 71501-1902-1 Urban Antioxidant Sunscreen SPF 40 50 mL in 1 BOTTLE, PLASTIC CREAM 50 4 71501-1902-2 Urban Antioxidant Sunscreen SPF 40 1.5 mL in 1 PACKET CREAM 1.5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71501-1902 URBAN ANTIOXIDANT SUNSCREEN SPF 40 (HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXYIDE CREAM) CREAM [DR. LORETTA, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20250417_930150a3-08bb-17fd-e053-2995a90a786b.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 71501-1902-1 71501190201 50 mL in 1 BOTTLE, PLASTIC (71501-1902-1) 50 ml 2019-09-16 0000-00-00 No No Current 71501-1902-2 71501190202 1.5 mL in 1 PACKET (71501-1902-2) 1.5 ml 2019-09-16 0000-00-00 No No Current