Home NDC 85164-005 HANCHOBIT Sunscreen
Product NDC 85164-005
11-digit product format 851640005
Labeler code 85164
Product ID 85164-005_449ff8f8-fe08-7bce-e063-6394a90ace56
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler HANCHOYEANBIOTEC Co.,Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-07
Substance BETULA ALBA JUICE
Active strength .01 mg/50mg
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 HANCHOBIT Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BETULA ALBA JUICE .01 mg/50mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9G931M6I4G 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 85164-005-01 HANCHOBIT Sunscreen 50 mg in 1 BOTTLE, PLASTIC CREAM 50 2
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 85164-005-01 85164000501 50 mg in 1 BOTTLE, PLASTIC (85164-005-01) 50 mg 2025-11-07 No No Current