Aiilo WART REMOVER - Guangzhou Huixue Biotechnology Co., Ltd.

Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Effective date
2026-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:53:40

Label at a glance#

ProductAiilo WART REMOVER
Active ingredientSALICYLIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 25%

INACTIVE INGREDIENT SECTION

Water, Borneol,Glycerin,Polyethylene Glycol, Bisabolol, Allantoin, Lonicera Japonica (Honeysuckle) Flower Extract, Sophora Angustifolia Root Extract.

OTC - PURPOSE SECTION

Wart remover

INDICATIONS & USAGE SECTION

Uses For the removal of warts, including plantar warts, flat warts, common warts, corns, and calluses.

WARNINGS SECTION

For external use only. Flammable Keep away from fire and flame. Keep out of reach of children. Avoid contact with eyes, in case of contact, flush eyes with plenty of cool water. Do not swallow, if swallowed, seek medical attention or contact a Poison Control Center (1-800-222-1222) immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Store af room temperature Avoid excessive heat above 37°C (99°F), Skin discoloration may occur during or after use.

OTC - WHEN USING SECTION

Wash affected area. Soak the wart in warm water for 5 minutes(optional). • Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry. Repeat these steps two to three times daily as needed (until the wart is removed) for up to 12 weeks.

OTC - DO NOT USE SECTION

On irritated skin or on any area that is infct . If you are allergic to any ingredient in this product. . On moles, birthmarks, warts with hair growing from them, genital warts or warts on the face or mucous membranes. .If you have diabetes or poor blood circulation. .If you are pregnant or breastfeeding unless directed by a healthcare practitioner.

OTC - STOP USE SECTION

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DOSAGE & ADMINISTRATION SECTION

Twice each day,(1ml)each time.15 days supply

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aiilo WART REMOVERAiilo WART REMOVER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87204-170-01Aiilo WART REMOVER30 mL in 1 BOTTLE, PLASTICLIQUID301

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87204-17087204-170-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
Aiilo WART REMOVERSALICYLIC ACID 25%Guangzhou Huixue Biotechnology Co., Ltd.4f17d170-a203-b8f3-e063-6294a90a09802026-04-10WarningsExact identifier
ndc (package): 87204-170-01
ndc (product): 87204-170
ndc11 (package): 87204017001
spl id: 4f17d170-a204-b8f3-e063-6294a90a0980
spl set id: 4f17d170-a203-b8f3-e063-6294a90a0980

Reported adverse events (FAERS/openFDA)#

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