Home NDC 84753-034 BISUTANG Sunscreen
Product NDC 84753-034
11-digit product format 847530034
Labeler code 84753
Product ID 84753-034_37fdb01b-929f-6a60-e063-6394a90a94e0
Type HUMAN OTC DRUG
Nonproprietary name BISUTANG Sunscreen
Dosage form LIQUID
Route CUTANEOUS
Labeler Guangdong Bisutang Biotechnology Co Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-20
Substance TITANIUM DIOXIDE
Active strength 3 g/3g
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 BISUTANG Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 3 g/3g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP 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 84753-034-01 BISUTANG Sunscreen 30 g in 1 BOTTLE, PLASTIC LIQUID 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 26 of 361 · 7,213 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84753-034-01 84753003401 30 g in 1 BOTTLE, PLASTIC (84753-034-01) 30 g 2025-06-20 No No Current