IBEALEE WART REMOVER liquid

iBeaLee Wart Remover by

Drug Labeling and Warnings

iBeaLee Wart Remover by is a Otc medication manufactured, distributed, or labeled by Shenzhen Yikai Electronic Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic acid 12%

Purpose

wart remover

Use

●for the removal of common and plantar warts

●the common wart is easily recognized by the rough”cauliflower-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 away from fire and flame.
only use on affected area.

Do not use

●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

When Using

● avoid contact with eyes. If the product gets into the eye,flush with water for 15 minutes
● avoid inhaling vapors

● cap the bottle tightly

●out of direct sunlight and store at room temperature away from heat

Stop Use

● 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.

Keep Oot Of Reach Of Children

Please store this product out of the reach of childre

Directions

● wash the affected area
●may soak the wart in warm water for 5 minutes · dry area thoroughly

● using the applicator(brush or cotton swab), apply one drop at a time to sufficiently cover each wart

● allow it to fully absorb and let dry
● repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IBEALEE WART REMOVER 
ibealee wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83809-002
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 mL

Inactive Ingredients
Ingredient Name	Strength
PODOPHYLLUM (UNII: 2S713A4VP3)
HIBISCUS SYRIACUS BARK (UNII: U6PQI719P3)
LONICERA HYPOGLAUCA FLOWER (UNII: 3ADI26ATFY)
CNIDIUM MONNIERI FRUIT OIL (UNII: JK0MS9P8YL)
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83809-002-01	5 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2023
2	NDC: 83809-002-02	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/20/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/20/2023

Labeler - Shenzhen Yikai Electronic Technology Co., Ltd. (700426808)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Yikai Electronic Technology Co., Ltd.		700426808	label(83809-002) , manufacture(83809-002)