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Hand Wash by Target Corp.

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Target Corp.
NDC Code: 11673-466

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

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
  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, fragrance, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 4, yellow 5

Questions?

Call 1-800-910-6874

Adverse reactions

Dist. by Target Corp., Mpls., MN 55403

Made in U.S.A. with U.S. and foreign components

2017 Target Brands, Inc

049 00 0646ROO

IDC-000274-01-069

466.001/466AB

principal display panel

antibacterial

foaming hand wash

up & up

helps fight

germs

40 FL OZ (1.18 L)

HAND WASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-466
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
COCAMIDOPROPYL BETAINE 
LAURAMIDOPROPYLAMINE OXIDE 
LAURAMINE OXIDE 
MYRISTAMIDOPROPYLAMINE OXIDE 
GLYCERIN 
CITRIC ACID MONOHYDRATE 
EDETATE SODIUM 
SULISOBENZONE 
FD&C RED NO. 4 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:11673-466-031479 mL in 1 BOTTLE, PLASTIC
2NDC:11673-466-571182 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/17/2016
Labeler - Target Corp. (006961700)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(11673-466)

 
Target Corp.

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Medically reviewed on Aug 7, 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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