TACRUITF 17% SALICYLIC ACID WART REMOVER SERUM- salicylic acid liquid

TACRUITF 17% Salicylic acid Wart Remover Serum by

Drug Labeling and Warnings

TACRUITF 17% Salicylic acid Wart Remover Serum by is a Otc medication manufactured, distributed, or labeled by Guangzhou Borderless Technology 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 and plantar warts.Common warts have a rough"cauliflower-like" surface and are easily recognizable.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, birthmarkswarts with hair growing from them, genital warts, or warts on the face or mucousmembranes.lf you have diabetesor poor blood circulation.

WHEN USING

Avoid contact with eyes. lf 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

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

1、Wash the affected area.

2、May soak wart in warm water for 5 minutes.Dry area thoroughly.

3、 Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry

4、 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

TACRUITF 17% SALICYLIC ACID WART REMOVER SERUM 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85304-010
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
WATER (UNII: 059QF0KO0R)
BORNEOL (UNII: M89NIB437X)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85304-010-01	2 in 1 PACKAGE	07/24/2025
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	505G(a)(3)	07/24/2025

Labeler - Guangzhou Borderless Technology Co., Ltd. (452282332)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Borderless Technology Co., Ltd.		452282332	manufacture(85304-010)