FDA.reportPublic FDA data

Kate Naturals Advanced Hand Sanitizer

Manufacturer
THE DOJO LLC
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:36

Label at a glance#

ProductKate Naturals Advanced Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure14 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

Store under 105F

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This hand sanitizer is manufactured using the following ingredients:

  1. Ethyl Alcohol (70%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Aloe Barbadensis Leaf
  3. Carbomer
  4. Dimethicone
  5. Triisopropanolamine
  6. Water

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop and persist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help promptly.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

  • Store under 105F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf, Carbomer, Dimethicone, Triisopropanolamine, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

237ml NDC: 75498-070-08

237ml Label237ml Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785ml NDC: 75498-070-01

3785ml Label3785ml Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

473ml NDC: 75498-070-16

473ml Label473ml Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75498-070-012022-01-28C16284748780-1d6a99b39-d6fc-a426-e053-dadaa90af4c2a359d3c8-59e7-5565-e053-2a95a90a3bad
75498-070-082022-01-28C16284748780-1d6a99b39-d6fc-a426-e053-dadaa90af4c2a359d3c8-59e7-5565-e053-2a95a90a3bad
75498-070-162022-01-28C16284748780-1d6a99b39-d6fc-a426-e053-dadaa90af4c2a359d3c8-59e7-5565-e053-2a95a90a3bad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75498-070-01Kate Naturals Advanced Hand Sanitizer3785 mL in 1 JUGGEL37851
75498-070-08Kate Naturals Advanced Hand Sanitizer237 mL in 1 BOTTLEGEL2371
75498-070-16Kate Naturals Advanced Hand Sanitizer473 mL in 1 BOTTLEGEL4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75498-070KATE NATURALS ADVANCED HAND SANITIZER (ALCOHOL) GEL [THE DOJO LLC]1Legacy NDC, 3 package rows20200417_a359d3c8-59e7-5565-e053-2a95a90a3bad.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75498-07075498-070-08, 75498-070-16, 75498-070-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 9404Q93RCW27EIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
DIMETHICONE 100RO266O364UIACT
FENOPROP TRIISOPROPANOLAMINE24FMI726KOIACT

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
a359d3c8-59d9-5565-e053-2a95a90a3bada359d3c8-59e7-5565-e053-2a95a90a3bad2020-04-15WarningsExact identifier
spl id: a359d3c8-59d9-5565-e053-2a95a90a3bad
spl set id: a359d3c8-59e7-5565-e053-2a95a90a3bad

Reported adverse events (FAERS/openFDA)#

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