FDA.reportPublic FDA data

MP. CODE INSTANT HAND SANITIZER 70% 100ml

Manufacturer
ARGO KOREA Co., Ltd | E.CIS Cosmetic Co.,Ltd
Effective date
2020-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:08

Label at a glance#

ProductMP. CODE INSTANT HAND SANITIZER 70% 100ml
Active ingredientALCOHOL
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(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Active Ingredient(s)Active Ingredient(s)

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

PurposePurpose

Use

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

UseUse

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

WarningWarning

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

Do not useDo not use

When using this product

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
When using this productWhen using this product

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Stop use and ask a doctorStop use and ask a doctor

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Keep out of reach of childrenKeep out of reach of children

Directions

DOSAGE & ADMINISTRATION 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.

DirectionsDirections

Other information

STORAGE AND HANDLING SECTION

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

Other InformationOther Information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Panthenol, Sodium Hyaluronate, Camellia Sinensis Leaf Extract

Inactive IngredientsInactive Ingredients

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MP. CODE
INSTANT
HAND SANITIZER
Help reduce bacteria on the skin
- For all day use
- Deep Moisturizing
- No Sticky
ETHYL ALCOHOL
70%
100ml / 3.38fl.oz.

Package Label - Principal Display PanelPackage Label - Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76887-106-032022-01-28C16284748780-1d6a99b39-cb54-a426-e053-dadaa90af4c2MP. CODE INSTANT HAND SANITIZER 100ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76887-106-01MP. CODE INSTANT HAND SANITIZER 70% 100ml100 mL in 1 BOTTLEGEL1001
76887-106-02MP. CODE INSTANT HAND SANITIZER 70% 100ml6 in 1 BOXGEL61
76887-106-03MP. CODE INSTANT HAND SANITIZER 70% 100ml60 in 1 CARTONGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76887-106MP. CODE INSTANT HAND SANITIZER 70% 100ML (ETHYL ALCOHOL) GEL [ARGO KOREA CO., LTD]1Legacy NDC, 3 package rows20201021_b216c3ae-5f9f-0d25-e053-2a95a90a5dfc.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76887-10676887-106-01, 76887-106-02, 76887-106-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PANTHENOLWV9CM0O67ZIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HYALURONATE SODIUMYSE9PPT4THIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
WATER059QF0KO0RIACT
GREEN TEA LEAFW2ZU1RY8B0IACT

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
b2164a37-01b9-4d67-e053-2995a90a22c6b216c3ae-5f9f-0d25-e053-2a95a90a5dfc2020-10-20WarningsExact identifier
spl id: b2164a37-01b9-4d67-e053-2995a90a22c6
spl set id: b216c3ae-5f9f-0d25-e053-2a95a90a5dfc

Reported adverse events (FAERS/openFDA)#

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