LIQUID WART CORN REMOVER- salicylic acid liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic acid 17%

PURPOSE

Wart remover

INDICATIONS & USAGE

For the removal of common warts and plantar warts. Common warts have a rough "cauliflower-like" surface and are easilyecognizable. Plantar warts are located only on the soles of the feet, tender to touch, with an interrupted footprint pattern.

WARNINGS

For external use only.

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. Non-edible.
Cap tightly and store at room temperature, away from heat.

STOP USE

Stop use and ask a doctorif discomfort persists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If 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 minutes.
Dry area thoroughly.Use a cotton swab to apply a sufficient amount to cover each wart. Letit dry.
Repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks.

INACTIVE INGREDIENT

Water
Polyethylene Glycol
Glycerin
Borneol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIQUID WART CORN REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87683-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.17 g  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87683-001-01	1 in 1 BOX	05/12/2026
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	05/12/2026

Labeler - Jiangxi Zhangling Industrial Co., Ltd. (408120639)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhangling Industrial Co., Ltd.		408120639	manufacture(87683-001)