DVO 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#

ProductDVO WART REMOVER
Active ingredientSALICYLIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 20%

INACTIVE INGREDIENT SECTION

Water, Borneol, Lactic Acid, Glycerin, Polyethylene Glycol, Bisabolol, Allantoin, Lonicera Japonica (Honeysuckle) Flower Extract, Sophora Augustifolia Root Extract, Hyaluronic Acid, Aloe Vera Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lithospermum Erythrorhizon 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.12 Weeks supply

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DVO WART REMOVERDVO WART REMOVER

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87204-172-01DVO WART REMOVER15 mL in 1 BOTTLE, PLASTICLIQUID151

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87204-17287204-172-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
DVO WART REMOVERSALICYLIC ACID 20%Guangzhou Huixue Biotechnology Co., Ltd.4f1c1098-241e-74b9-e063-6394a90afff72026-04-10WarningsExact identifier
ndc (package): 87204-172-01
ndc (product): 87204-172
ndc11 (package): 87204017201
spl id: 4f1c1098-241f-74b9-e063-6394a90afff7
spl set id: 4f1c1098-241e-74b9-e063-6394a90afff7

Reported adverse events (FAERS/openFDA)#

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