Home NDC 85163-019 OUHOE Water-Permeable Sunscreen
Product NDC 85163-019
11-digit product format 851630019
Labeler code 85163
Product ID 85163-019_46e63e1e-7852-ca26-e063-6394a90a9b53
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE
Dosage form SPRAY
Route TOPICAL
Labeler Shantou Ouhoe Technology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-27
Substance ARTEMISIA ARGYI LEAF
Active strength .01 mg/100mg
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 OUHOE Water-Permeable Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARTEMISIA ARGYI LEAF .01 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2JYC99Q0WZ 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 85163-019-01 OUHOE Water-Permeable Sunscreen 100 mg in 1 BOTTLE, SPRAY SPRAY 100 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 81 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85163-019-01 85163001901 100 mg in 1 BOTTLE, SPRAY (85163-019-01) 100 mg 2025-12-27 No No Current