MQUPIN CORN REMOVAL PADS- corn removal pads patch

MQUPIN Corn Removal Pads by

Drug Labeling and Warnings

MQUPIN 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,calluses and common warts
relieves pain by removing corns and calluses

Warnings

■ For external use only

■Keep away from fire and flame

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.

Stop Use

discomfort persists

Ask Doctor

Ask a doctor before use if you have

■diabetes

■ poor blood circulation

Keep Out Of Reach Of Children

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 and and dry the area Remove bandage strips by peeling backing off

■lf 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 weeks

Other information

■ store between 20°to 25°C (68° to 77°F)

Inactive ingredients

hard paraffin,lanolin,phenol

Questions

mqupin86@gmail.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MQUPIN CORN REMOVAL PADS 
corn removal pads patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83781-001
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)
LANOLIN (UNII: 7EV65EAW6H)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83781-001-01	24 in 1 BOX; Type 0: Not a Combination Product	11/05/2023
2	NDC: 83781-001-02	38 in 1 BOX; Type 0: Not a Combination Product	11/05/2023
3	NDC: 83781-001-03	48 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	manufacture(83781-001) , label(83781-001)