ZOURUNAN WART REMOVER- wart remover liquid

zourunan WART REMOVER by

Drug Labeling and Warnings

zourunan WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Guchutang Biotechnology (Longyan) Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic acid 6 % v/v

Purpose

wart remover

Use

·For the removal of common and plantar warts
·The common wart is easily recognized by the rough “cauliflower-like"appearance on the surface,
·The plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the footprint pattern.

Warnings

For external use only. Flammable.
Keep away from fire and flame.

Do not use

·On irritated skin or on any area that is infected or reddened
·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.

When Using

·Avoid contact with eyes.If product gets into the eye, flush with water for 15 minutes.
·Avoid inhaling vapors

·Cap tightly and store at room temperature away from heat.

Stop Use

if discomfort persists

Ask Doctor

if discomfort persists

Keep Out Of Reach Of Children

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

Directions

·Wash affected area·may soak wart in warm water for 5 minutes.
·Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry.
·Repeat this procedure once or twice daily as needed (until wart is removed)for up to 12 weeks.

Other information

·Store at room temperature
·Avoid excessive heat 37℃ (99℉)
·Skin discoloration may accur during or after use

Inactive ingredients

Purified Water, Magnesium Chloride, Phenytoin, Caramel, Propylene Glycol, Sodium Hydroxide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZOURUNAN WART REMOVER 
wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87083-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CARAMEL (UNII: T9D99G2B1R)
PHENYTOIN (UNII: 6158TKW0C5)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87083-005-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	11/06/2025

Labeler - Guchutang Biotechnology (Longyan) Co., Ltd (456645111)

Establishment
Name	Address	ID/FEI	Business Operations
Guchutang Biotechnology (Longyan) Co., Ltd		456645111	manufacture(87083-005)