MI DEURIUM ANTIBACTERIAL WET WIPES- glyceryl laurate liquid

Mi Deurium Antibacterial Wet Wipes by

Drug Labeling and Warnings

Mi Deurium Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by SEOJEON CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Glyceryl laurate 10%

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only

Do not use

● in children less than 2 months of age

● on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

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

● Place enough product on hands to cover all surfaces. Rub hands together until dry.

● Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

● Store between 15-30C (59-86F)

● Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

purified water, sodium coco pg-dimonium chloride phosphate, methylpropanediol, laurylpyridinium chloride, caprylhydroxamic acid, alcohol, levulinic acid, sodium levulinate

Package Label

INGREDIENTS AND APPEARANCE

MI DEURIUM ANTIBACTERIAL WET WIPES 
glyceryl laurate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79542-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERYL LAURATE (UNII: Y98611C087) (GLYCERYL LAURATE - UNII:Y98611C087)	GLYCERYL LAURATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
LEVULINIC ACID (UNII: RYX5QG61EI)
SODIUM LEVULINATE (UNII: VK44E1MQU8)
LAURYLPYRIDINIUM CHLORIDE (UNII: KJM5A6A3YL)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79542-201-01	40 g in 1 POUCH; Type 0: Not a Combination Product	07/10/2020
2	NDC: 79542-201-02	80 g in 1 POUCH; Type 0: Not a Combination Product	07/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/10/2020

Labeler - SEOJEON CO., LTD (694781990)

Registrant - SEOJEON CO., LTD (694781990)

Establishment
Name	Address	ID/FEI	Business Operations
SEOJEON CO., LTD		694781990	manufacture(79542-201)