MYMULIKE CORN REMOVAL PADS- corn removal pads patch

MYMULIKE Corn Removal Pads by

Drug Labeling and Warnings

MYMULIKE Corn Removal Pads by is a Otc medication manufactured, distributed, or labeled by Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic acid 40%

Purpose

Corn and callus remover

Use

for the removal of corns from foot and hand.

Warnings

for external use only

Do not use

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

When Using

if product gets in eyes,flush with water for 15 minutes.
Ask a doctor before use if you have

■diabetes

■poor blood circulation

■under 14 years old

■pregnant and lactating women

Stop Use

discomfort persists.

Ask Doctor

discomfort persists.

Keep Out Of Reach Of Children

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

Directions

■Wash affected corn and dry thoroughly.

■Please cut the medicated patch as a suitable size to cover your corn.

■Place frmly the medicated round part over the center of corn. Adhesive next to skin.

■Repeart the treatment as need until corn is removed. (The result may vary from person.)

■May soak corn in warm water for 5 minutes to assist in the removal.

Other information

store between 20°to 25℃ (68°to 77℉)

Inactive ingredients

hard paraffin, lanolin, phenol

Questions

MYMULIKE@gmail.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MYMULIKE CORN REMOVAL PADS 
corn removal pads patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83781-003
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
PARAFFIN (UNII: I9O0E3H2ZE)
PHENOL (UNII: 339NCG44TV)
LANOLIN (UNII: 7EV65EAW6H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83781-003-01	24 in 1 BOX; Type 0: Not a Combination Product	11/05/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	11/05/2023

Labeler - Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd (701762807)

Establishment
Name	Address	ID/FEI	Business Operations
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd		701762807	label(83781-003) , manufacture(83781-003)