Total Sanitizer Alcohol Free Hand Saniting Foam

Manufacturer
Total Sanitizer, LLC
Effective date
2020-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:07

Label at a glance#

ProductTotal Sanitizer Alcohol Free Hand Saniting Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

For handwashing to decrease bacteria on the skin. After changing diapers. After assisting ill persons. Before contact with a person under medical care or treatment. Recommended for repeat use.

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under six years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin.
  • After changing diapers.
  • After assisting ill persons.
  • Before contact with a person under medical care or treatment.
  • Recommended for repeat use.

Warnigns

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs. rinse thoroughly with water.

Stop use and ask a doctorif

OTC - STOP USE SECTION

irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under six years of age should be supervised when using this product.

Other information

SPL UNCLASSIFIED SECTION

  • Store in a cool, dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Juice, Polysorbate 20, Glycerin, Potassium Sorbate, Fragrnace, Citric Acid, Disodium EDTA, Tocopheryl Acetate (Vitamin E).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046310benzalkonium chloride 0.12 % Topical FoamPSN1
1046310benzalkonium chloride 1.2 MG/ML Topical FoamSCD1
1046310benzalkonium chloride 0.12 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80463-003-002022-07-29C16284748780-1e4f33bdf-a2b2-d8a0-e053-dadaa90a6e4eTotal Sanitizer Alcohol Free Hand Saniting Foam

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80463-003-00Total Sanitizer Alcohol Free Hand Saniting Foam3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80463-003TOTAL SANITIZER ALCOHOL FREE HAND SANITING FOAM (BENZALKONIUM CHLORIDE) LIQUID [TOTAL SANITIZER, LLC]1Legacy NDC, 1 package rows20200912_aefaf972-3932-400c-e053-2a95a90aeab0.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
80463-00380463-003-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
aefaf972-3933-400c-e053-2a95a90aeab0aefaf972-3932-400c-e053-2a95a90aeab02020-09-10WarningsExact identifier
spl id: aefaf972-3933-400c-e053-2a95a90aeab0
spl set id: aefaf972-3932-400c-e053-2a95a90aeab0

Reported adverse events (FAERS/openFDA)#

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