FDA.reportPublic FDA data

Kuri Hand Sanitizer

Manufacturer
Kuri Enterprises
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:23

Label at a glance#

ProductKuri Hand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

 Wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin, only when water is not available.

Warnings

WARNINGS SECTION

-Flammable, Keep away from heat or flame

-For external use only.

When using this product

OTC - WHEN USING SECTION

  • Do not get into eyes
  • If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation and redness develop

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

  •  Wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, Acrylates/dimethicome copolymer, Methylchloroisothiazolinone, Methylisothiazolinone, Triethanolamine, Aloe Vera Extract

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79560-001-012022-01-28C16284748780-1d6a99b39-f7cb-a426-e053-dadaa90af4c2Kuri Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79560-001-01Kuri Hand Sanitizer250 mL in 1 BOTTLELIQUID2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79560-001KURI HAND SANITIZER (ALCOHOL) LIQUID [KURI ENTERPRISES]1Legacy NDC, 1 package rows20200715_aa6ad389-08ac-577f-e053-2a95a90a02ec.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79560-00179560-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

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
aa6ac2c0-b98f-1f0f-e053-2a95a90aff6baa6ad389-08ac-577f-e053-2a95a90a02ec2020-07-14WarningsExact identifier
spl id: aa6ac2c0-b98f-1f0f-e053-2a95a90aff6b
spl set id: aa6ad389-08ac-577f-e053-2a95a90a02ec

Reported adverse events (FAERS/openFDA)#

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