ELSOPHIE WART CORN REMOVER- wart corn remover liquid liquid

Elsophie Wart Corn Remover by

Drug Labeling and Warnings

Elsophie Wart Corn Remover by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xinxin Yunhai Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

salicylic acid 17%

Purpose

corn wart treatment

Use

Corns, calluses, flat warts, plantar warts, common warts less than 5 mm

Warnings

For external use only, avoid contact with the face or healthy skin, flush with water immediately of it gets into your eyes.

Do not use

on eyes area

When Using

for external use only, avoid contact with the face or healthy skin, flush with water immediately of it gets into your eyes.

Stop Use

If you are allergic to this product, if symptoms persist for over 7 days or worsen,consult your physicaian.

Ask Doctor

If you are allergic to this product, if symptoms persist for over 7 days or worsen,consult your physicaian.

Keep Out Of Reach Of Children

​Keep Out Of Reach Of Children

Directions

soak the corn warts with warm water for 5 minutes, install the brush into the bottle cap,press tightly, dry the skin and open the lid, dip the liquid and applyu it on the wart or corn with the brush wait for a mask to form then apply the liquid again. use twice during day and twice at night, use it for 2 weeks unbtil the skin recover its health. if corns or warts are big, it may take a long time

Other information

Store at room temperature (15–30°C/59–86°F).

Avoid exposure to direct sunlight or excessive heat.

Inactive ingredients

Fructus cnidii, podophyllum hexandrum, hawthorn, stellera chamaejasme linn, sophora flavescens，Cortex Pseudolaricis，Honeysuckle

Questions

For more information, contact VINER INC. at:

Address: 742 South Meadow St, Suite 200, Ithaca, NY 14850, USA.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ELSOPHIE WART CORN REMOVER 
wart corn remover liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83818-021
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
RUBUS CHINGII WHOLE (UNII: A32A8VI76N)
PODOPHYLLUM HEXANDRUM WHOLE (UNII: 0E1BZ0WZXH)
AQUILEGIA CANADENSIS WHOLE (UNII: 636VYW51FP)
STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
CRATAEGUS MONOGYNA FLOWER (UNII: NT52AMP29J)
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83818-021-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	07/30/2025

Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xinxin Yunhai Technology Co., Ltd.		699816806	manufacture(83818-021)