DVO WART REMOVER- salicylic acid 20% liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 20%

INACTIVE INGREDIENT

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.

PURPOSE

Wart remover

INDICATIONS & USAGE

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

WARNINGS

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.

KEEP OUT OF REACH OF CHILDREN

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

WHEN USING

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.

DO NOT USE

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.

STOP USE

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

DOSAGE & ADMINISTRATION

Twice each day,(1ml)each time.12 Weeks supply

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DVO WART REMOVER 
salicylic acid 20% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87204-172
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BORNEOL (UNII: M89NIB437X)
LACTIC ACID (UNII: 33X04XA5AT)
GLYCERIN (UNII: PDC6A3C0OX)
BISABOLOL (UNII: 24WE03BX2T)
HYALURONIC ACID (UNII: S270N0TRQY)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87204-172-01	15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/10/2026	04/14/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	04/10/2026	04/14/2027

Labeler - Guangzhou Huixue Biotechnology Co., Ltd. (418186127)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Huixue Biotechnology Co., Ltd.		418186127	manufacture(87204-172)