MI DEURIUM ANTIBACTERIAL WET WIPES- glyceryl laurate liquid 
SEOJEON CO., LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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

79542-201-01

79542-201-01

79542-201-02

79542-201-02

MI DEURIUM ANTIBACTERIAL WET WIPES 
glyceryl laurate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79542-201
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERYL LAURATE (UNII: Y98611C087) (GLYCERYL LAURATE - UNII:Y98611C087) GLYCERYL LAURATE10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79542-201-0140 g in 1 POUCH; Type 0: Not a Combination Product07/10/2020
2NDC:79542-201-0280 g in 1 POUCH; Type 0: Not a Combination Product07/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/10/2020
Labeler - SEOJEON CO., LTD (694781990)
Registrant - SEOJEON CO., LTD (694781990)
Establishment
NameAddressID/FEIBusiness Operations
SEOJEON CO., LTD694781990manufacture(79542-201)

Revised: 12/2023
Document Id: 0d8c8187-20b2-54ec-e063-6394a90ac5a0
Set id: aa0dd3d7-c762-2a1f-e053-2995a90a7a79
Version: 4
Effective Time: 20231228
 
SEOJEON CO., LTD