Magic wipes by MIGO G.N.R. TRADING LTD / HARDAL GLOBAL CONSULTING LLC Hand wipes

Magic wipes by

Drug Labeling and Warnings

Magic wipes by is a Otc medication manufactured, distributed, or labeled by MIGO G.N.R. TRADING LTD, HARDAL GLOBAL CONSULTING LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MAGIC WIPES- alcohol cloth 
MIGO G.N.R. TRADING LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand wipes

Active Ingredient(s)

Ethyl Alcohol 5%, Benzalkonium Chloride 0.125%

Purpose

Antiseptic

Use

Use for hand-washing to decrease bacteria on the skin, only when water is not available.

Warnings

Flammable. Keep away from heat and flames. For external use only.

When using this product do not get into eyes if contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands thoroughly with the product and allow to dry without wiping.

Other information

Keep pack tightly closed when not in use. Store in a cool and dry place.

Inactive ingredients

Water 93.875%, Glycerin 1.000%, Lemon Essence.

Disposal

Dispose the wipes and packaging in accordance to local legislation. Do not flush wipes down the toilet.

Package Label - Principal Display Panel

Magic wipes

For a perfect cleaning

Daily Use

Disinfecting Antibacterial Hand Wipes

• Kills 99.9% of virus & bacteria
• Defend against MRSA, Norovirus, E. Coli & many more
• Disinfects & Sanitizes

Contact: Magic Wipes

1253 Coney Island ave. Brooklyn, NY 11230

magicwipes2020@gmail.com

(917) 861-3525

Made in Turkey

Distributed by:

MiGo GNR Trading Ltd.

Nakash 8 st., Petach-Tikva, Israel, 4976002

MAGIC WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80727-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.125 g  in 100 g
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80727-001-02	386 g in 1 BOX; Type 0: Not a Combination Product	03/30/2020
2	NDC: 80727-001-01	2251 g in 1 BOX; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020	12/30/2021

Labeler - MIGO G.N.R. TRADING LTD (531832689)

Registrant - HARDAL GLOBAL CONSULTING LLC (123584960)

Establishment
Name	Address	ID/FEI	Business Operations
MIGO G.N.R. TRADING LTD		531832689	label(80727-001)

Revised: 9/2020

Document Id: b07aabba-88c2-3f5b-e053-2995a90a3bf9

34390-5

Set id: b07aab20-ff72-9686-e053-2995a90a9f3e

Version: 1

Effective Time: 20200929