WART REMOVER- salicylic acid ointment

Wart Remover by

Drug Labeling and Warnings

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

Drug Details [pdf]

ASK DOCTOR

If discomfort persists

If you have diabetes or poor blood circulation

DO NOT USE

on warts with hair growing from them, on moles, birthmarks, or genital warts

on irritated skin or on any area that is infected or reddened

KEEP OUT OF REACH OF CHILDREN

If swallowed,seek immediate medical attention

PURPOSE

wart remover

WHEN USING

avoid contact with eyes. lf the product gets into the eyes, flush with water for 15minutes
avoid inhaling vapors
do not apply to irritated skin

INDICATIONS & USAGE

Wash the affected area
May soak the wart in warm water for 5 minutes.
Dry area thoroughly.
Using the applicator, coat the wart with a thin layer of ointment to sufficiently covereach wart.
Allow it to fully absorb and cover it with a bandage as needed.Repeat this procedure once or twice daily as needed (until the wart is removed) forup to 12 weeks.

DOSAGE & ADMINISTRATION

15 ml

WARNINGS

Keep away from fire and flame; For external use only

INACTIVE INGREDIENT

Water, Centella Asiatica Extract, Purslane Extract, Tea Tree Oil, Jojoba Seed Oil, Glycerin

ACTIVE INGREDIENT

salicylic acid 10%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER 
salicylic acid ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87276-261
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CENTELLA ASIATICA (UNII: 7M867G6T1U)
JOJOBA OIL (UNII: 724GKU717M)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PURSLANE (UNII: M6S840WXG5)
TEA TREE OIL (UNII: VIF565UC2G)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87276-261-01	1 g in 1 TUBE; Type 0: Not a Combination Product	02/04/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	02/04/2026

Labeler - Shenzhen Zhenshangzekai Technology Co., Ltd. (518601007)