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Hand Wash by Permatex

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3091mg in 1mL
Labeler: Permatex
NDC Code: 70616-743

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.

Fast Orange Antibacterial Foaming Hand Wash

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

´╗┐Warnings

For external use only: hands only

When using this product
  • avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if
  • irritation or redness develops
  • 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
  • apply palmful to dry hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

water, glycerin, lauramine oxide, cocamidopropyl betaine, PEG-150 distearate, cocamide MEA, frgrance, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, blue 1, red 33

PERMATEX and design are TMs of Illinois Tool Works, Inc. 2016 Permatex, a division of ITW.

Solon, OH 44139/  Assembled in U.S.A. with U.S. and global materials

www.permatex. com Item # 95105

Principal Display Panel

FAST ORANGE

Antibacterial FOAMING HAND WASH

FRESH SCENT!

Helps kill harmful germs

Gentle enough for everyday use

7.5 FL OZ (221 mL)

743.000/743AA/628AC

HAND WASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70616-743
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3091 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
LAURAMINE OXIDE 
COCAMIDOPROPYL BETAINE 
PEG-150 DISTEARATE 
COCO MONOETHANOLAMIDE 
CITRIC ACID MONOHYDRATE 
EDETATE SODIUM 
DMDM HYDANTOIN 
SULISOBENZONE 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:70616-743-96221 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/12/2016
Labeler - Permatex (964477025)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(70616-743)

Revised: 08/2017
 
Permatex

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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