Home NDC 84019-047 WART REMOVER
Product NDC 84019-047
11-digit product format 840190047
Labeler code 84019
Product ID 84019-047_58e901b8-66e1-d2d6-e063-6394a90ae601
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form SOLUTION
Route TOPICAL
Labeler Shengnan (Guangzhou) Cosmetics Co., LTD
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-13
Substance SALICYLIC ACID
Active strength 40 g/100mL
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 40 g/100mL
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 2741040 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 7 of 56 · 1,101 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84019-047-01 84019004701 30 mL in 1 BOTTLE (84019-047-01) 30 ml 2026-08-13 No No Current