Tork Hand Washing Antibacterial Foam

Manufacturer
Essity Professional Hygiene North America LLC | Nice-Pak Products, LLC
Effective date
2026-02-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:36:37

Label at a glance#

ProductTork Hand Washing Antibacterial Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Indications and uses

handwashing to help decrease bacteria on the skin recommended for repeated use

Dosage and administration

wet hands, dispense enough to cover both hands, rub for 30 seconds then rinse with clean water for 30 seconds

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • handwashing to help decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
  • do not ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more then 72 hours

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, dispense enough to cover both hands, rub for 30 seconds then rinse with clean water for 30 seconds

Inactive ingredients 

INACTIVE INGREDIENT SECTION

water, caprylyl/capryl glucoside, laurtrimonium chloride, cocamidopropylamine oxide, lauryl glucoside, citric acid, methylcholorisothiazonlinone, methylisothiazolinone

Questions or comments?

OTC - QUESTIONS SECTION

1-866-722-8675

Disclaimer

SPL UNCLASSIFIED SECTION

NOT FOR SALE

Can be ordered as:

401815 for S4, 1000ml

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills 99.9% of Common Germs*

*based on majority of microorganisms tested under ASTM E2783-11 in 30 seconds

NDC 49351-304-02

TORK ®

SAMPLE - NOT FOR SALE

Tork Antimicrobial Hand Washing Foam Soap

Benzalkonium Chloride 0.13%

1.5 FL OZ (44 mL)

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN8
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD8
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY8
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49351-304-01Tork Hand Washing Antibacterial Foam1000 mL in 1 BOTTLESOAP10008
49351-304-02Tork Hand Washing Antibacterial Foam44 mL in 1 BOTTLESOAP448

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
49351-30449351-304-01, 49351-304-02

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
Tork Hand Washing Antibacterial FoamBENZALKONIUM CHLORIDEEssity Professional Hygiene North America LLC0f72f0cb-9e8e-43bb-862e-0024771ece1b2026-02-04Warnings, Adverse reactionsExact identifier
ndc (package): 49351-304-02
ndc (package): 49351-304-01
ndc (product): 49351-304
ndc11 (package): 49351030401
ndc11 (package): 49351030402
spl id: 4a03411e-4fc7-1ce1-e063-6394a90aa752
spl set id: 0f72f0cb-9e8e-43bb-862e-0024771ece1b

Reported adverse events (FAERS/openFDA)#

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