Home NDC 84989-007 XIMONTH Liquid Wart Corn Callus Remover
Product NDC 84989-007
11-digit product format 849890007
Labeler code 84989
Product ID 84989-007_448b773c-6dd7-db23-e063-6294a90a4c4a
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form LIQUID
Route TOPICAL
Labeler Shantou Ximonth Biotechnology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-17
Substance MELALEUCA ALTERNIFOLIA LEAF; GINGER
Active strength .006; .006 mg/30mg; mg/30mg
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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 XIMONTH Liquid Wart Corn Callus Remover
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MELALEUCA ALTERNIFOLIA LEAF .006 mg/30mg GINGER .006 mg/30mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G43C57162K Internal UNII lookup C5529G5JPQ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84989-007-01 XIMONTH Liquid Wart Corn Callus Remover 30 mg in 1 BOTTLE LIQUID 30 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 28 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 84989-007-01 84989000701 30 mg in 1 BOTTLE (84989-007-01) 30 mg 2025-07-17 No No Current