DVO WART REMOVER

Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Effective date
2026-01-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:36:10

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% V/V

INACTIVE INGREDIENT SECTION

Water, Borneol, Glycerin, Polyethylene Glycol, Bisabolol, Allantoin, Lonicera Japonica (Non-eysuckle) Flower Extract, Sophora Augustifolia Root Extract.

OTC - PURPOSE SECTION

Wart remover

INDICATIONS & USAGE SECTION

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

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.

WARNINGS SECTION

Foexternal use only Flammrable, Keen away from fire and flame. Keep out of reach of children. Avoid contact with eyes. In case of contact, flush eyes with glenty of cool water. Do not swallow. If swatowed, seek medieol ottention or contactPeioon Gontret Center (1-800-222-1222) immediataly.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children should use this product under adult supervision .

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

Fosexternal use only Flammable. Keep away from fire and flame. Keep out oreach of children Avoid contact with eyes. In case of contact, flush eyes withglenty of cool water. . Do not swallow. If swatowed, seek medielottentien orconteetionGontret Center (1-800-222-1222) immediately. Other Warnings 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 - DO NOT USE SECTION

On irritated skin or on any area that is infected or reddened. • 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. yhavediabetespoorod ccuation, . If you are pregnant or breastfeeding unless directed by a healthcare practitioner.

OTC - STOP USE SECTION

Discontinue use and consult a doctor if: .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

DVO WART REMOVERDVO WART REMOVER

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87204-162-01DVO WART REMOVER30 g 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
87204-16287204-162-01

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
DVO WART REMOVERSALICYLIC ACID 20% V/VGuangzhou Huixue Biotechnology Co., Ltd.499ca27c-5760-8016-e063-6294a90aa5ae2026-01-30WarningsExact identifier
ndc (package): 87204-162-01
ndc (product): 87204-162
ndc11 (package): 87204016201
spl id: 499ca27c-5761-8016-e063-6294a90aa5ae
spl set id: 499ca27c-5760-8016-e063-6294a90aa5ae

Reported adverse events (FAERS/openFDA)#

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