Home NDC 84019-036 SKIN TAG REMOVER
Product NDC 84019-036
11-digit product format 840190036
Labeler code 84019
Product ID 84019-036_3ee79d66-e729-48dd-e063-6394a90a6463
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form LIQUID
Route CUTANEOUS
Labeler Shengnan (Guangzhou) Cosmetics Co., LTD
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-16
Substance SALICYLIC ACID
Active strength 100 mg/g
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 SKIN TAG REMOVER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 100 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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84019-036-01 SKIN TAG REMOVER 20 g in 1 BOTTLE LIQUID 20 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 38 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84019-036-01 84019003601 20 g in 1 BOTTLE (84019-036-01) 20 g 2025-09-16 No No Current