Home NDC 87204-201 Okkazhie WART REMOVER
Product NDC 87204-201
11-digit product format 872040201
Labeler code 87204
Product ID 87204-201_59c2d759-d1ea-6c9d-e063-6294a90a04db
Type HUMAN OTC DRUG
Nonproprietary name 40% SALICYLIC ACID
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Huixue Biotechnology Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-16
Marketing end 2027-08-21
Substance SALICYLIC ACID
Active strength .4 mg/30mL
NDC exclude flag No
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 Okkazhie WART REMOVER Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID .4 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 8 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 87204-201-01 87204020101 30 mL in 1 BOTTLE, PLASTIC (87204-201-01) 30 ml 2026-08-16 2027-08-21 No No Historical