Home NDC 84989-021 AKOLKOL TOENAIL FUNGUS TREATMENT
Product NDC 84989-021
11-digit product format 849890021
Labeler code 84989
Product ID 84989-021_5121c341-e5ea-2b36-e063-6394a90a93b8
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 2026-05-06
Substance ALOE BARBADENSIS LEAF; CENTELLA ASIATICA LEAF
Active strength .003; .003 mg/30mg; mg/30mg
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 AKOLKOL TOENAIL FUNGUS TREATMENT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALOE BARBADENSIS LEAF .003 mg/30mg CENTELLA ASIATICA LEAF .003 mg/30mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ZY81Z83H0X Internal UNII lookup 6810070TYD 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 84989-021-01 AKOLKOL TOENAIL FUNGUS TREATMENT 30 mg in 1 BOTTLE, PLASTIC LIQUID 30 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 55 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 84989-021-01 84989002101 30 mg in 1 BOTTLE, PLASTIC (84989-021-01) 30 mg 2026-05-06 No No Current