FDA.reportPublic FDA data

LaRose Kills Germs Hand Sanitizing Wipes

Manufacturer
LaRose Industries DBA Cra-Z-Art | LaRose Industries d/b/a Cra-Z-Art
Effective date
2021-08-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:36:44

Label at a glance#

ProductLaRose Kills Germs Hand Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

• Thoroughly wipe hands with cloth • Rub hands together until dry • No rinsing required

Storage and handling

• Dispose of properly, do not flush

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use:

INDICATIONS & USAGE SECTION

• Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

Do not use if you are allergic to any of the ingredients

When using this product
• Avoid getting into the eyes.
• In case of eye contact, immediately flush eyes thoroughly with water.

Stop use and ask a doctor if
• Irritation or redness develops
• Conditions persist for more than 72 hours
• Redness is present

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

• Thoroughly wipe hands with cloth
• Rub hands together until dry
• No rinsing required

Other information

STORAGE AND HANDLING SECTION

• Dispose of properly, do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid, fragrance.

SPL UNCLASSIFIED SECTION

ADVANCED FORMULA

NEW!

* SANITIZE & MOISTURIZE

* GENTLE ON HANDS

KILLS 99.99% OF GERMS

© 2020 LaRose Industries, LLC. All Rights Reserved.

LaRose Industries, LLC, Randolph, NJ 07869 USA.

At LaRose, we guarantee our quality. If you are not completely satisfied with our product, please call 1-800-272-9278

Made in the USA of domestic and imported materials.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73836-31973836-319-40, 73836-319-80

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
fde1e615-da47-4211-8bee-bc8707e984ed5a947376-075d-4c70-abc0-0dd503e8f7f22021-08-26WarningsExact identifier
spl id: fde1e615-da47-4211-8bee-bc8707e984ed
spl set id: 5a947376-075d-4c70-abc0-0dd503e8f7f2

Reported adverse events (FAERS/openFDA)#

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