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; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
80; 50; 50; 80 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Urban Antioxidant Sunscreen SPF 40
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE80 mg/mL
OCTOCRYLENE50 mg/mL
ZINC OXIDE50 mg/mL
OCTISALATE80 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV06SV4M95S, 5A68WGF6WM, SOI2LOH54Z, 4X49Y0596W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71501-1902-1Urban Antioxidant Sunscreen SPF 4050 mL in 1 BOTTLE, PLASTICCREAM504
71501-1902-2Urban Antioxidant Sunscreen SPF 401.5 mL in 1 PACKETCREAM1.54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71501-1902URBAN ANTIOXIDANT SUNSCREEN SPF 40 (HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXYIDE CREAM) CREAM [DR. LORETTA, LLC]4Current NDC, Legacy NDC, 2 package rows20250417_930150a3-08bb-17fd-e053-2995a90a786b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71501-1902-17150119020150 mL in 1 BOTTLE, PLASTIC (71501-1902-1) 50 ml2019-09-160000-00-00NoNoCurrent
71501-1902-2715011902021.5 mL in 1 PACKET (71501-1902-2) 1.5 ml2019-09-160000-00-00NoNoCurrent