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Antibacterial Hand Wash by Vi-Jon, Inc

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, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 33, red 40, yellow 5

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 
LAURAMINE OXIDE 
COCAMIDOPROPYL BETAINE 
LAURAMIDOPROPYLAMINE OXIDE 
SODIUM CHLORIDE 
myristamidopropylamine oxide 
GLYCERIN 
DISTEARETH-75 ISOPHORONE DIISOCYANATE 
PEG-150 distearate 
CITRIC ACID MONOHYDRATE 
EDETATE SODIUM 
SULISOBENZONE 
SODIUM BENZOATE 
D&C RED NO. 33 
FD&C RED NO. 40 
FD&C YELLOW NO. 5 
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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Medically reviewed on Aug 27, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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