Mi Deurium Antibacterial Wet Wipes

Manufacturer
SEOJEON CO., LTD
Effective date
2023-12-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:05:49

Label at a glance#

ProductMi Deurium Antibacterial Wet Wipes
Active ingredientGLYCERYL LAURATE
Label structure12 sections

Dosage and administration

● 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.

Storage and handling

● Store between 15-30C (59-86F) ● Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Glyceryl laurate 10%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

DOSAGE & ADMINISTRATION SECTION

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

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

● in children less than 2 months of age

● on open skin wounds

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

● 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

STORAGE AND HANDLING SECTION

● Store between 15-30C (59-86F)

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79542-201-0179542-201-01

79542-201-0179542-201-01

79542-201-0279542-201-02

79542-201-0279542-201-02

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79542-201-012025-01-30C16284748780-12cef2736-5ffc-d83d-e063-dadaa90ab31faa0dd3d7-c762-2a1f-e053-2995a90a7a79
79542-201-022025-01-30C16284748780-12cef2736-5ffc-d83d-e063-dadaa90ab31faa0dd3d7-c762-2a1f-e053-2995a90a7a79

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79542-201-01Mi Deurium Antibacterial Wet Wipes40 g in 1 POUCHLIQUID404
79542-201-02Mi Deurium Antibacterial Wet Wipes80 g in 1 POUCHLIQUID804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79542-201MI DEURIUM ANTIBACTERIAL WET WIPES (GLYCERYL LAURATE) LIQUID [SEOJEON CO., LTD]4Legacy NDC, 2 package rows20231228_aa0dd3d7-c762-2a1f-e053-2995a90a7a79.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79542-20179542-201-01, 79542-201-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0d8c8187-20b2-54ec-e063-6394a90ac5a0aa0dd3d7-c762-2a1f-e053-2995a90a7a792023-12-28WarningsExact identifier
spl id: 0d8c8187-20b2-54ec-e063-6394a90ac5a0
spl set id: aa0dd3d7-c762-2a1f-e053-2995a90a7a79

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.