Drug Labeling and Warnings

Drug Details

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TORK FOAM ANTIBACTERIAL- benzalkonium chloride soap 
Essity Professional Hygiene North America LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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

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.)

Tork Label2.jpg

TORK FOAM ANTIBACTERIAL 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 49351-104
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCO GLUCOSIDE (UNII: ICS790225B)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 49351-104-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/15/2017
Labeler - Essity Professional Hygiene North America LLC (005694349)
Registrant - CYAN Labs S.A. de C.V. (812754130)
Establishment
NameAddressID/FEIBusiness Operations
CYAN Labs S.A. de C.V.812754130manufacture(49351-104) , label(49351-104) , pack(49351-104)

Revised: 8/2019
 
Essity Professional Hygiene North America LLC


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