TORK FOAM ANTIBACTERIAL- benzalkonium chloride soap

Tork Foam Antibacterial by

Drug Labeling and Warnings

Tork Foam Antibacterial by is a Otc medication manufactured, distributed, or labeled by Essity Professional Hygiene North America LLC, CYAN Labs S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium chloride, 0.13%

Purpose

Antiseptic

Uses

• For hand washing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

When using this

product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

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

Directions

• Pump a small amount of foam into palm of hand  
• Rub thoroughly over all surfaces of both hands for 15 seconds
• Rinse with potable water

Inactive ingredients

Water/Eau/Aqua, Coco-glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric acid.

Questions or Comments?

1-866-722-8675

PRINCIPAL DISPLAY PANEL

TORK®

Foam Soap

Antibacterial

NDC: 49351-104-01

Manufactured for Essity Professional Hygiene North America, LLC

2929 Arch Street

Philadelphia, PA 19104

www.torkusa.com

For Commercial use

Made in Mexico

Premium

1 L

(33.8 US fl. oz.)

(35.2 oz. liq.)

INGREDIENTS AND APPEARANCE

TORK FOAM ANTIBACTERIAL 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49351-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCO GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49351-104-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2017
2	NDC: 49351-104-02	24 in 1 BOX	03/15/2017
2		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/15/2017

Labeler - Essity Professional Hygiene North America LLC (005694349)

Registrant - CYAN Labs S.A. de C.V. (812754130)

Establishment
Name	Address	ID/FEI	Business Operations
CYAN Labs S.A. de C.V.		812754130	manufacture(49351-104) , label(49351-104) , pack(49351-104)