TORK HAND WASHING ANTIBACTERIAL FOAM- benzalkonium chloride soap

Tork Hand Washing Antibacterial Foam by

Drug Labeling and Warnings

Tork Hand Washing Antibacterial 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

• handwashing 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 develope 
• condition persists for more then 72 hours

Keep out of reach of children.

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

Directions

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

Inactive ingredients 

water//equ/aqua, caprylyl/capryl glucoside, laurtrimonium chloride, cocamidopropylamine oxide, lauryl glucoside, citric acid

Questions or comments?

1-866-722-8675

Adverse reaction

TORK

essity

Manufactured for 

Essity Professional Hygiene North America LLC

2929 Arch Street

Philadelphia, Pennsylvania 19104

www.essity.com, www.torkusa.com

Made in USA of Domestic and Imported Components 

Patents: www.essity.com/patents

Principal Panel Display

Kills 99.9% of Common Germs*

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

TORK

NDC: 49351-304-01

Tork Antibacterial Hand

Washing Foam Soap

Benzalkonium Chloride 0.13%

NSF

Nonfood Compounds Program Listed E2 167747

40 18 15

S4

1L

(33.8 FL OZ)

Peel Here

INGREDIENTS AND APPEARANCE

TORK HAND WASHING ANTIBACTERIAL FOAM 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49351-304
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)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49351-304-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2023
2	NDC: 49351-304-02	44 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/27/2023

Labeler - Essity Professional Hygiene North America LLC (005694349)

Registrant - Consumer Product Partners, LLC (119091514)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(49351-304)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(49351-304)