FDA.reportPublic FDA data

AKOLKOL TOENAIL FUNGUS TREATMENT - Shantou Ximonth Biotechnology Co., Ltd.

Manufacturer
Shantou Ximonth Biotechnology Co., Ltd.
Effective date
2026-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:56:03

Label at a glance#

ProductAKOLKOL TOENAIL FUNGUS TREATMENT
Active ingredientALOE BARBADENSIS LEAF, CENTELLA ASIATICA LEAF
Label structure12 sections

Storage and handling

This product should be stored in a cool, dry place,away from direct sunlight and high temperatures

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ALOE BARBADENSIS LEAF EXTRACT、CENTELLA ASIATICA LEAF EXTRACT

OTC - PURPOSE SECTION

For the effective treatment of nail discoloration,thickening, splitting, crumbling, and brittleness

OTC - WHEN USING SECTION

1: Wash and dry affected nails thoroughly before
bedtime.
2: Use the pipette to apply 2-3 drops of oil evenly to affected areas.
3: Visible results in as few as 7 days.

WARNINGS SECTION

Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children.

STORAGE AND HANDLING SECTION

This product should be stored in a cool, dry place,away from direct sunlight and high temperatures

INACTIVE INGREDIENT SECTION

AQUA、GLYCERIN、OUBAKU EKISU

INDICATIONS & USAGE SECTION

1: Wash and dry affected nails thoroughly before
bedtime.
2: Use the pipette to apply 2-3 drops of oil evenly to affected areas.
3: Visible results in as few as 7 days.

DOSAGE & ADMINISTRATION SECTION

1: Wash and dry affected nails thoroughly before
bedtime.
2: Use the pipette to apply 2-3 drops of oil evenly to affected areas.
3: Visible results in as few as 7 days.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84989-021-01AKOLKOL TOENAIL FUNGUS TREATMENT30 mg in 1 BOTTLE, PLASTICLIQUID301

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84989-02184989-021-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
PHELLODENDRON AMURENSE BARKPBG27B754GIACT
ALOE BARBADENSIS LEAFZY81Z83H0XACTIB
AQUA059QF0KO0RIACT
CENTELLA ASIATICA LEAF6810070TYDACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AKOLKOL TOENAIL FUNGUS TREATMENTGLYCERINShantou Ximonth Biotechnology Co., Ltd.5121c341-e5e9-2b36-e063-6394a90a93b82026-05-06WarningsExact identifier
ndc (package): 84989-021-01
ndc (product): 84989-021
ndc11 (package): 84989002101
spl id: 5121c341-e5ea-2b36-e063-6394a90a93b8
spl set id: 5121c341-e5e9-2b36-e063-6394a90a93b8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.