WART REMOVER by Shenzhen Mengyue Technology Co., Ltd. WART REMOVER liquid

WART REMOVER by

Drug Labeling and Warnings

WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Shenzhen Mengyue Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 17%

PURPOSE

Wart remover

INDICATIONS & USAGE

USES
To remove warts such as plantar wart, flat wart, common wart and corns, calluses.
The plantar wart is recognized by its location only on the bottom of the foot it's tenderness, and the interruption of the footprint pattern.

WARNINGS

WARNINGS

· The liquid can get easily volatilized & crystallized, tighten the cap after use.

· Avoid long-term contact with air while using.

· For external use only, don't contact with eyes or swallow.Children should use it under the supervision of adults.

DO NOT USE

DO NOT USE

On damaged skin(cuts, abrasions, eczema, sunburn.

If you are allergic to any of the ingredients in this product.

If you are pregnant or breastfeeding.

WHEN USING

N/A

STOP USE

ASK DOCTOR

See a doctor as you may have a more serious skin condition.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACHOF CHILDREN

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

DOSAGE & ADMINISTRATION

DIRECTIONS

Wash the affected area.

May soak the wart in warm water for 5 minutes.

Dry area thoroughly.

Using the applicator(cotton swab),apply a layer of ointment to sufficiently cover each 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) for up to 12 weeks.

STORAGE AND HANDLING

OTHER INFORMATION:

Store between 68°F to 77°F(20°C to 25°C).

Protect from excessive heat above 104°F(40°C).

INACTIVE INGREDIENT

INACTIVE INGREDIENTS
Shard paraffin, lanolin, phenol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER 
wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87255-003
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
PHENOL (UNII: 339NCG44TV)
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87255-003-01	15 mL in 1 BOX; Type 0: Not a Combination Product	11/13/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	11/13/2025

Labeler - Shenzhen Mengyue Technology Co., Ltd. (511200055)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Mengyue Technology Co., Ltd.		511200055	manufacture(87255-003)