Home NDC 84019-046 WART REMOVER
Product NDC 84019-046
11-digit product format 840190046
Labeler code 84019
Product ID 84019-046_58d245c3-c686-5784-e063-6294a90a1e23
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form PATCH
Route CUTANEOUS
Labeler Shengnan (Guangzhou) Cosmetics Co., LTD
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-12
Substance SALICYLIC ACID
Active strength 400 mg/g
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 WART REMOVER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 400 mg/g
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 240559 Internal RxNorm 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 55 · 1,088 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84019-046-01 84019004601 180 g in 1 BOTTLE (84019-046-01) 180 g 2026-08-12 No No Current