LK Hand Sanitizer (Ethanol)

Manufacturer
Venice Cosmetic
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:13:08

Label at a glance#

ProductLK Hand Sanitizer (Ethanol)
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

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

Dosage and administration

Take appropriate amount onto your hand and spread it all the way to fingertips. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Uses

INDICATIONS & USAGE SECTION

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

Purpose

OTC - PURPOSE SECTION

Antibacterial

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

  • if you are allergic to any of the ingredients
  • in children less than 2 months of age
  • on open skin wounds

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

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

If pregnant or breast-feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Take appropriate amount onto your hand and spread it all the way to fingertips. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

LK Hand Sanitizer (Ethanol)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

lk hand sanitizerlk hand sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809392803198GTIN-13: 8809392803198
EAN-13: 8809392803198
GTIN storage (14 digits): 08809392803198
lk hand sanitizer.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74488-013-012022-01-28C16284748780-1d6a99b39-720f-a426-e053-dadaa90af4c2LK Hand Sanitizer (Ethanol)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74488-013-01LK Hand Sanitizer (Ethanol)500 mL in 1 BOTTLE, SPRAYLIQUID5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74488-013LK HAND SANITIZER (ETHANOL) (ALCOHOL) LIQUID [VENICE COSMETIC]2Legacy NDC, 1 package rows20200515_a58af034-dfc0-37a6-e053-2995a90a0396.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74488-01374488-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
a5a104e3-3abe-187b-e053-2995a90a9beca58af034-dfc0-37a6-e053-2995a90a03962020-05-14WarningsExact identifier
spl id: a5a104e3-3abe-187b-e053-2995a90a9bec
spl set id: a58af034-dfc0-37a6-e053-2995a90a0396

Reported adverse events (FAERS/openFDA)#

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