Home NDC 73071-101 DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN
Product NDC 73071-101
11-digit product format 730710101
Labeler code 73071
Product ID 73071-101_41a7173d-db1a-19df-e063-6294a90a3b31
Type HUMAN OTC DRUG
Nonproprietary name Octocrylene, Homosalate, Octisalate, Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler DEWYTREE CO. ,LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-26
Substance OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Active strength 2.4; 3.6; 4.9; 1.5 g/50mL; g/50mL; g/50mL; g/50mL
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 DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 2.4 g/50mL HOMOSALATE 3.6 g/50mL OCTOCRYLENE 4.9 g/50mL AVOBENZONE 1.5 g/50mL
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 73071-101-01 DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN 1 in 1 BOX CREAM 1 2 73071-101-02 DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN 50 mL in 1 TUBE CREAM 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73071-101 DEWYTREE URBAN SHADE HYALURONIC LIGHTWEIGHT SUNSCREEN (OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE) CREAM [DEWYTREE CO. ,LTD] 1 Current NDC, 2 package rows 20250328_2f1ca6e0-f689-57c7-e063-6394a90a3da5.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 73071-101-01 73071010101 1 TUBE in 1 BOX (73071-101-01) / 50 mL in 1 TUBE (73071-101-02) 1 tube 2025-03-26 No No Current 73071-101-02 73071010102 50 mL in 1 TUBE 50 ml Historical