WART REMOVER- wart remover patches patch

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 40%

PURPOSE

Wart Remover

INDICATIONS & USAGE

Use

For the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface.

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

On irritated, infected or reddened skin

On genital warts and warts on the face

On moles, birthmarks and warts with hair growing from them

On mucous membranes

WHEN USING

When using

Ask a doctor before use if you have diabetes or poor blood circulation.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

DOSAGE & ADMINISTRATION

Directions

·Wash affected area may soak wart in warm water for 5 minutes

·Dry area thoroughly

·Remove bandage strips by peeling back off

·If necessary, cut medicated patch to fit wart

·Carefully apply medicated plaster

·Repeat procedure every 48 hours as needed(until wart is removed) for up to 12 weeks

STORAGE AND HANDLING

Other information

Store between 59° and 86°F (15° and 30° C).

INACTIVE INGREDIENT

Inactive ingredientsHard paraffin, lanolin, phenol, borneol, crocus sativus L, gleditsia sinensis Lam

DOSAGE & ADMINISTRATION

Dosage&administration section

One patch per day, each patch contains 12 mg of salicylic acid.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER 
wart remover patches patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87255-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	40 g  in 100

Inactive Ingredients
Ingredient Name	Strength
PHENOL (UNII: 339NCG44TV)
PARAFFIN (UNII: I9O0E3H2ZE)
GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)
CROCUS SATIVUS WHOLE (UNII: Z5C927G4XF)
BORNEOL (UNII: M89NIB437X)
LANOLIN (UNII: 7EV65EAW6H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87255-004-01	144 in 1 BOX; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	12/01/2025

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

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Mengyue Technology Co., Ltd.		511200055	manufacture(87255-004)