Peunitory WART REMOVER

Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Effective date
2026-03-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:50:39

Label at a glance#

ProductPeunitory WART REMOVER
Active ingredientSALICYLIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 40%

INACTIVE INGREDIENT SECTION

Water, Borneol, Glycerin, Polyethylene Glycol, Bisabolol, Allantoin, Lonicera Japonica (Honeysuckle) Flower Extract, Sophora Augustifolia Root Extract, Hyaluronic Acid, Aloe Vera Extract.

OTC - PURPOSE SECTION

Wart remover

INDICATIONS & USAGE SECTION

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. Children should use this product under adult supervision. Avoid prolonged exposure to air during use as the substance may dissolve and crystallize easily. Recap immediately after each use, Do not use if the cap is broken or missing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - WHEN USING SECTION

1,Clean the affected area, You can soak the affected area in warm water for 5 minutes (optional). 2. Dip the liquid with the brush and apply iton the affected area. Ensure complete coverage. Let it dry. 3. Repeat this process 2-3 times daily until the skin looks smooth. 4. More severe may require more time.Patience and perseverance are required during its use. The longest continuous use period is no more than 12 weeks.

OTC - STOP USE SECTION

You become pregnant or are trying to become pregnant while using this product. •Irritation or redness occurs, worsens, or does not improve with continued use.

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Peunitory Fungal Nail TreatmentPeunitory Fungal Nail Treatment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87204-168-01Peunitory 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 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87204-16887204-168-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Peunitory WART REMOVERSALICYLIC ACID 40%Guangzhou Huixue Biotechnology Co., Ltd.4d24df93-b18a-b4c2-e063-6394a90ae0622026-03-16WarningsExact identifier
ndc (package): 87204-168-01
ndc (product): 87204-168
ndc11 (package): 87204016801
spl id: 4d24df93-b18b-b4c2-e063-6394a90ae062
spl set id: 4d24df93-b18a-b4c2-e063-6394a90ae062

Reported adverse events (FAERS/openFDA)#

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