WART REMOVER- salicylic acid 17% liquid

WART REMOVER by

Drug Labeling and Warnings

WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Shenzhen Haizhida E-commerce Co., Ltd, Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 17%

PURPOSE

Wart remover

INDICATIONS & USAGE

For the removal of common warts andplantar warts.Common warts have a rough "cauliflower-like" surface and are easily recognizablePlantar warts are located only on the solesofthe feet, tender to touch, with aninterrupted footprint pattern.

WARNINGS

For external use only.

DO NOT USE

on irritated skin or on any area that isinfected or reddened.On moles, birthmarks.warts with hair growing from them,genital warts, or warts on the face ormucous membranes.lf you have diabetesor poor blood circulation.

WHEN USING

Avoid contact with eyes. lf product getsinto the eye, flush with Water for 15minutes.Non-edible.Cap tightly and store at room temperature,away from heat.

STOP USE

Stop use and ask a doctor if discomfort persists.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contactthe Poison Control Center (1-800-222-1222)right away.

DOSAGE & ADMINISTRATION

Wash the affected area.
May soak wart in warm water for 5 minutes.
Dry area thoroughly.
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.

INACTIVE INGREDIENT

Water
Polyethylene Glycol
Borneol
Glycerin
Podofilox

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER 
salicylic acid 17% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85825-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	17 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PODOFILOX (UNII: L36H50F353)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BORNEOL (UNII: M89NIB437X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85825-003-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	06/23/2025

Labeler - Shenzhen Haizhida E-commerce Co., Ltd (509640283)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(85825-003)