VKAVKA WART REMOVER- salicylic acid liquid

vkavka Wart Remover by

Drug Labeling and Warnings

vkavka Wart Remover by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lanxi Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic acid 12%

PURPOSE

wart remover

INDICATIONS & USAGE

Effectively removes both common warts and plantar warts
Common warts are identified by their raised, rough texture resembling a cauliflower's surface
Plantar warts specifically occur on weight-bearing areas of the foot, typically causing pressure pain when walking and noticeable disruption of the natural foot skin ridge patterns

WARNINGS

Use only on the skin surface.

Keep away from fire and flame

Precise application: Cover only the wart, not surrounding skin

DO NOT USE

on irritated skin or on any area that is infected or reddened.
on moles, birthmarks, warts with hair growing from them, warts on the face or mucous membranes.
lf you have a known hypersensitivity disorder or diabetes mellitus or poor blood circulation.

WHEN USING

Avoid contact with eyes. lf the product gets into the eye,flush with water for 15 minutes.
Avoid inhaling vapors.
Cap tightly and store at room temperature, away from heat.
Non-edible.

STOP USE

lf discomfort persists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.lf swallowed get medical help or contact the Poison Control Center(1-800-222-1222)right away.

DOSAGE & ADMINISTRATION

Wash the affected area.
May soak wart in warm water for 5 minutese
Dry area thoroughly.
Use a brush to apply a sufficient amount to cover each wart.
Allow it to fully absorb and let dry .
Repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.

INACTIVE INGREDIENT

Water
Sophora flavescens root
Cnidium monnieri whole
Hawthorn leaf with flower
Podophyllum
Stellera chamaejasm whole
Borneol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VKAVKA WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87386-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.12 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PODOPHYLLUM (UNII: 2S713A4VP3)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)
CNIDIUM MONNIERI WHOLE (UNII: GYR30735RE)
BORNEOL (UNII: M89NIB437X)
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87386-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	01/29/2026

Labeler - Shenzhen Lanxi Trading Co., Ltd. (512086574)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lanxi Trading Co., Ltd.		512086574	manufacture(87386-001)