FDA.reportPublic FDA data

VT Hand Sanitizer 500ml

Manufacturer
EL Kingdom | E.CIS Cosmetic Co.,Ltd
Effective date
2020-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:13

Label at a glance#

ProductVT Hand Sanitizer 500ml
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Active Ingredient(s)Active Ingredient(s)

Purpose

OTC - PURPOSE SECTION

Antiseptic

PurposePurpose

Use

INDICATIONS & USAGE SECTION

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

UseUse

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

WarningsWarnings

Do not use

OTC - DO NOT USE SECTION

in children less than 2 month of age on open skin wounds

on open skin wounds

Do not useDo not use

OTC - WHEN USING SECTION

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

When using sectionWhen using section

OTC - STOP USE SECTION

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

Stop use sectionStop use section

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 children sectionKeep out of reach of children section

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children when using this product to avoid swallowing.

DirectionsDirections

Other information

STORAGE AND HANDLING SECTION

Store between 15°C to 30°C(59°F to 86°F)

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

Other informationOther information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Fragrance(Parfum), Carbomer, Aminomethyl Propanol, Sodium Hyaluronate, Panthenol, Scutellaria Baicalensis Root Extract, Portulaca Oleracea Extract, Aloe Barbadensis Leaf Extract

Inactive ingredientsInactive ingredients

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

THINK

YOUR

LIFE

VT GAND SANITIZER

NON-STERILE SOLUTION

ETHANOL 70%

16.9 fl. oz. / 500 ml

VTº

Package LabelPackage Label

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
80013-000-022022-01-28C16284748780-1d6a99b39-c715-a426-e053-dadaa90af4c2VT Hand Sanitizer 500ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80013-000-01VT Hand Sanitizer 500ml500 mL in 1 BOTTLE, PLASTICGEL5001
80013-000-02VT Hand Sanitizer 500ml24 in 1 CARTONGEL241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80013-000VT HAND SANITIZER 500ML (ETHYL ALCOHOL) GEL [EL KINGDOM]1Legacy NDC, 2 package rows20200820_ac417005-7b36-c89b-e053-2995a90a4c54.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80013-00080013-000-01, 80013-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYLPROPANOLLU49E6626QIACT
PURSLANEM6S840WXG5IACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
HYALURONATE SODIUMYSE9PPT4THIACT
PANTHENOLWV9CM0O67ZIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
ac417005-7b37-c89b-e053-2995a90a4c54ac417005-7b36-c89b-e053-2995a90a4c542020-08-06WarningsExact identifier
spl id: ac417005-7b37-c89b-e053-2995a90a4c54
spl set id: ac417005-7b36-c89b-e053-2995a90a4c54

Reported adverse events (FAERS/openFDA)#

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