FDA.reportPublic FDA data

Hello Kitty Hand Sanitizer

Manufacturer
The Dial Corporation, a Henkel company
Effective date
2015-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:44:01

Label at a glance#

ProductHello Kitty Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

OTC - PURPOSE SECTION

Antibacterial

INDICATIONS & USAGE SECTION

  • Hand Sanitizer

WARNINGS SECTION

  • For external use only
  • Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

avoid contact with face, eyes, and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INSTRUCTIONS FOR USE SECTION

Wet hands thoroughly with product and rub into skin until dry

SPL UNCLASSIFIED SECTION

Children under 6 years of age should be supervised by an adult when using this product.

INACTIVE INGREDIENT SECTION

Water (Aqua), Hydroxyethyl Urea, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol, Fragrance (parfume), Red 33 (CI 17200)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back LabelBack LabelFront labelFront label

OTC - QUESTIONS SECTION

1-800-258-3425

DOSAGE & ADMINISTRATION SECTION

Topical liquid

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN1
247835ethanol 0.62 ML/ML Topical SolutionSCD1
247835ethanol 62 % Topical SolutionSY1
247835ethyl alcohol 62 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54340-256-012020-01-31C16284748780-19d75b9d0-8053-f424-e053-dadaa90a57ce1c7061bd-dcc5-1b13-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-256-01Hello Kitty Hand Sanitizer59 mL in 1 BOTTLE, DISPENSINGLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54340-256HELLO KITTY HAND SANITIZER (HAND SANITIZER) LIQUID [THE DIAL CORPORATION, A HENKEL COMPANY]1Legacy NDC, 1 package rows20151112_1c7061bd-dcc5-1b13-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-25654340-256-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
1c7061bd-dcc6-1b13-e054-00144ff88e881c7061bd-dcc5-1b13-e054-00144ff88e882015-08-03WarningsExact identifier
spl id: 1c7061bd-dcc6-1b13-e054-00144ff88e88
spl set id: 1c7061bd-dcc5-1b13-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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