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

Questions or comments?

1-866-722-8675

Disclaimer

NOT FOR SALE

Can be ordered as:

401815 for S4, 1000ml

Adverse reaction

essity

Manufactured for 

Essity Professional Hygiene North America LLC

2929 Arch Street

Philadelphia, Pennsylvania 19104

www.essity.com, www.torkusa.com

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

NDC: 49351-304-02

TORK ®

SAMPLE - NOT FOR SALE

Tork Antimicrobial Hand Washing Foam Soap

Benzalkonium Chloride 0.13%

1.5 FL OZ (44mL)

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)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

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)