Home NDC 85064-014-01 WART REMOVER
Product NDC 85064-014
Requested package NDC 85064-014-01
11-digit product format 850640014
Labeler code 85064
Product ID 85064-014_448e4aeb-09c8-2de6-e063-6294a90a96ba
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form PATCH
Route TOPICAL
Labeler Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-28
Substance TEA TREE OIL
Active strength .9 mg/180mg
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 WART REMOVER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TEA TREE OIL .9 mg/180mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VIF565UC2G 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 85064-014-01 WART REMOVER 180 mg in 1 PATCH PATCH 180 2
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 58 of 68 · 1,346 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85064-014-01 85064001401 180 mg in 1 PATCH (85064-014-01) 180 mg 2025-09-28 No No Current