FDA.reportPublic FDA data

PURETIZE INSTANT HAND SANITIZER 70% 250ml

Manufacturer
ARGO KOREA Co., Ltd | E.CIS COSMETIC.Co.,Ltd
Effective date
2020-05-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:14:55

Label at a glance#

ProductPURETIZE INSTANT HAND SANITIZER 70% 250ml
Active ingredientALCOHOL
Label structure13 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 ingredientsactive ingredients

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

WarningsWarnings

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

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 usingWhen using

Stop use

OTC - STOP USE SECTION

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

Stop useStop use

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 outKeep out

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, Sodium Hyaluronate, Panthenol, Gardenia Jasminoides Fruit Extract

Inactive ingredientsInactive ingredients

Questions or Comments?

OTC - QUESTIONS SECTION

Toll Free: 1-844-756-3784

QuestionsQuestions

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PURETIZE
INSTANT

HAND SANITIZER

FIGHTS TO REDUCE GERMS

FOR ALL DAY USE

DEEP MOISTURIZING

REFRESHING ALOE

ETHYL ALCOHOL

70%

250ml/ 8.45fl.oz

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76887-103-022022-01-28C16284748780-1d6a99b39-a7ab-a426-e053-dadaa90af4c2PURETIZE INSTANT HAND SANITIZER 70% 250ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76887-103-01PURETIZE INSTANT HAND SANITIZER 70% 250ml250 mL in 1 BOTTLE, PUMPGEL2503
76887-103-02PURETIZE INSTANT HAND SANITIZER 70% 250ml36 in 1 CARTONGEL363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76887-103PURETIZE INSTANT HAND SANITIZER 70% 250ML (ETHYL ALCOHOL) GEL [ARGO KOREA CO., LTD]3Legacy NDC, 2 package rows20200528_a467b392-a175-397c-e053-2995a90a2c20.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76887-10376887-103-01, 76887-103-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
PANTHENOLWV9CM0O67ZIACT
GARDENIA JASMINOIDES FRUIT7CTH8MD549IACT
CARBOMER 9404Q93RCW27EIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYALURONATE SODIUMYSE9PPT4THIACT

Source Document#

Source XML · Source PDF

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
a6ae6e53-4e6d-77d0-e053-2995a90a7b70a467b392-a175-397c-e053-2995a90a2c202020-05-28WarningsExact identifier
spl id: a6ae6e53-4e6d-77d0-e053-2995a90a7b70
spl set id: a467b392-a175-397c-e053-2995a90a2c20

Reported adverse events (FAERS/openFDA)#

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