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Antibacterial Hand Wash by Vi-Jon, Inc

Medically reviewed on June 7, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.313mg in 1mL
Labeler: Vi-Jon, Inc
NDC Code: 11344-488

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.

Drug facts

Active ingredient section

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands

When using this product
  • avoid contact with the eyes.  If contact occurs, rinse eyes 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
  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

water, cocamidopropyl betaine, lauramine oxide, PEG-150 distearate, sodium chloride, cetrimonium chloride, decyl glucoside, glycerin, fragrance, disteareth-75 IPDI, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, yellow 5, red 40, red 33

Adverse Reactions

DISTRIBUTED BY: VI-JON, INC., ST. LOUIS, MO 63114

488.002/488AC

Principal Display Panel

germ-X

ANTIBACTERIAL

HAND WASH

1150 mL (39 FL OZ)

ANTIBACTERIAL HAND WASH 
benzalkonium chloride 0.13% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-488
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.313 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
COCAMIDOPROPYL BETAINE 
LAURAMINE OXIDE 
PEG-150 DISTEARATE 
SODIUM CHLORIDE 
CETRIMONIUM CHLORIDE 
decyl glucoside 
GLYCERIN 
DISTEARETH-75 ISOPHORONE DIISOCYANATE 
CITRIC ACID MONOHYDRATE 
EDETATE SODIUM 
DMDM HYDANTOIN 
SULISOBENZONE 
FD&C YELLOW NO. 5 
FD&C RED NO. 40 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:11344-488-07750 mL in 1 BOTTLE, PLASTIC
2NDC:11344-488-271150 mL in 1 BOTTLE, PLASTIC
3NDC:11344-488-083785 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/27/2016
Labeler - Vi-Jon, Inc (150931459)
Registrant - Vi-Jon, Inc (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon. nc150931459manufacture(11344-488)

 
Vi-Jon, Inc

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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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