WART REMOVER PATCH patch

Wart Remover Patch by

Drug Labeling and Warnings

Wart Remover Patch by is a Otc medication manufactured, distributed, or labeled by Shenzhen Hengkaifeng Commerce and Trade Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic acid

Purpose

wart remover

Uses

Use

● for the removal of common and plantar warts

● the common wart is easily recognized by the roughcauliflower-like appearance of the surface

● the plantar wart is recognized by its location only on the bottom of the foot,its tenderness and the interruption of the footprint pattern

Warnings

For external use only.
Keep this and all drugs out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Stop using this product and see your doctor if discomfort persists for more than 72 hours

When using this product :

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

●on moles, birthmarks, warts with hair growing from them, warts on the face or mucous membranes

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

Directions Of Safe Use:

● wash affected area and dry thoroughly apply tag patch after 24 hours. remove tag patch

● repeat procedure every 24 hours for up to 14 days for tags /warts removal and up to 12 weeks for warts, until the problem hascleared.

● may hot compress wart in warm water for 5 minutes to assist in removal

Stop use and ask a doctor:

· if discomfort persists.·if you have diabetes
or poor blood circulation.Keep out of reach
of children. lf swallowed, get medical help
or contact a Poison Control Center right
away.

Inactive ingredients

Cnidium monnieri, Podophyllum,Hawthorn, Stellera chamaejasm, Sophora flavescens, Earthy hibiscus bark, Honeysuckle

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER PATCH 
wart remover patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84117-044
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	12 g  in 100

Inactive Ingredients
Ingredient Name	Strength
PODOPHYLLUM (UNII: 2S713A4VP3)
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)
HIBISCUS SYRIACUS BARK (UNII: U6PQI719P3)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
CNIDIUM MONNIERI FRUIT OIL (UNII: JK0MS9P8YL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84117-044-01	180 in 1 BOX; Type 0: Not a Combination Product	04/22/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	04/22/2025

Labeler - Shenzhen Hengkaifeng Commerce and Trade Co., Ltd (444722774)