Home NDC 87357-001-01 sunscreen
Product NDC 87357-001
Requested package NDC 87357-001-01
11-digit product format 873570001
Labeler code 87357
Product ID 87357-001_48f13b1c-8105-881b-e063-6394a90a816d
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE
Dosage form LOTION
Route CUTANEOUS
Labeler Guangdong Zhoubang Biotechnology Co., Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-22
Substance TITANIUM DIOXIDE; ETHYLHEXYL SALICYLATE
Active strength 2.85; 3 g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 2.85 g/100mL ETHYLHEXYL SALICYLATE 3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup 4X49Y0596W 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 87357-001-01 sunscreen 30 mL in 1 BOTTLE, GLASS LOTION 30 1
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 162 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87357-001-01 87357000101 30 mL in 1 BOTTLE, GLASS (87357-001-01) 30 ml 2026-01-22 No No Current