TORK HAND SANITIZING ALCOHOL-FREE FOAM- benzalkonium chloride liquid

Tork Hand Sanitizing Alcohol-Free Foam by

Drug Labeling and Warnings

Tork Hand Sanitizing Alcohol-Free Foam by is a Otc medication manufactured, distributed, or labeled by Essity Professional Hygiene North America LLC, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride, 0.13%

Purpose

Antiseptic

Uses

• Hand Sanitizer to help decrease bacteria on the skin.
• Recommended for repeated use

Warnings

For external use only

Do not use

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

When using this product

• 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

• irritation and redness develop
• condition persists more than 72 hours

Keep out of reach of children:

if swallowed, get medial help or contact a Posion Control Center right away.

Directions

Dispense enough to spread on both hands to wrists, then rub into skin for 30 seconds. Allow to dry.

Inactive ingredients

water, lactic acid, phenoxyethanol, sodium hydroxide, propylene glycol, cocamidopropyl betaine, sodium cocoamphoacetate

Questions or comments?

1-866-722-8675

SPL UNCLASSIFIED SECTION

essity

Manufactured for

Essity Professional Hygiene

North America LLC

2929 Arch Street

Philadelphia, Pennsylvania 19104

www.essity.com, www.torkusa.com

Made in USA from Domestic & Imported Components 

Patents/Brevets/Patentes: www.essisty.com/patents

NOT FOR SALE

Can be ordered as: 401813 for S4, 1000ml

Principal panel display

Kills 99.9% of Common Germs*

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

NDC: 49351-303-02

TORK ®

Tork Hand Sanitizing

Alcohol-Free Foam

Benzalkonium Chloride, 0.13%

1.5 FL OZ (44 mL)

INGREDIENTS AND APPEARANCE

TORK HAND SANITIZING ALCOHOL-FREE FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49351-303
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LACTIC ACID (UNII: 33X04XA5AT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49351-303-02	44 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/18/2022
2	NDC: 49351-303-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/18/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/18/2022

Labeler - Essity Professional Hygiene North America LLC (005694349)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(49351-303)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(49351-303)