VENISHOO MY1CART HAND SANITIZER

Manufacturer
VENISHOO Co.,Ltd
Effective date
2020-09-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:19

Label at a glance#

ProductVENISHOO MY1CART HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ethanol

OTC - PURPOSE SECTION

■ sterilization of hands and skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Water, Alcohol,Butylene Glycol,
Polyoxyethylene, Glycerin, Carbomer, Fragrance, Triethanolamine

INDICATIONS & USAGE SECTION

wet hands thoroughly with product and allow to dry without wiping

for children under 6, use only under adult supervision

not recommended for infants

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78075-0002-12022-01-28C16284748780-1d6a99b39-9549-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78075-0002-1VENISHOO MY1CART HAND SANITIZER500 mL in 1 BOTTLELIQUID, EXTENDED RELEASE5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78075-0002VENISHOO MY1CART HAND SANITIZER (ALCOHOL) LIQUID, EXTENDED RELEASE [VENISHOO CO.,LTD]1Legacy NDC, 1 package rows20200915_af43a3c5-fff0-66ce-e053-2a95a90a8e43.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78075-000278075-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
af43c788-39c7-d60e-e053-2a95a90ac5fcaf43a3c5-fff0-66ce-e053-2a95a90a8e432020-09-14WarningsExact identifier
spl id: af43c788-39c7-d60e-e053-2a95a90ac5fc
spl set id: af43a3c5-fff0-66ce-e053-2a95a90a8e43

Reported adverse events (FAERS/openFDA)#

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