WART REMOVER PATCHS- wart remover patch

WART REMOVER PATCHS by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic acid 20%

PURPOSE

Wart Remover

USE

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

WARNINGS

For external use only.

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

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

wash affected area: may soak wart in warm water for 5 minutes
dry area thoroughly
remove bandage strips by peeling backing 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 week

WHEN USING

Ask a doctor before use if you have
diabetes poor blood circulatio

OTHER INFORMATION

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

INACTIVE INGREDIENTS

Ethylhexyl Acrylate ·Polyethylene Terephthalate

DOSAGE & ADMINISTRATION SECTION

One patch per day, each patch contains1 mg of tolnaftate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER PATCHS 
wart remover patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84168-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	200 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)	380 mg  in 1 g
POLYETHYLENE TEREPHTHALATE (INTRINSIC VISCOSITY 0.40-0.70) (UNII: Y78AJD3DED)	420 mg  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84168-015-11	16.8 g in 1 BOX; Type 0: Not a Combination Product	05/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	05/09/2024

Labeler - Gaozhou Chapin Technology Co., Ltd (715573719)

Establishment
Name	Address	ID/FEI	Business Operations
Gaozhou Chapin Technology Co., Ltd		715573719	manufacture(84168-015)