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Hand Sanitizer by Target Corp

Medically reviewed on December 11, 2017

Dosage form: gel
Ingredients: ALCOHOL 567mg in 1mL
Labeler: Target Corp
NDC Code: 11673-086

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.

Hand Sanitizer Kiwi Punch

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Use
  • to decrease bacteeria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only-hands

Flammable. Keep away from heat and flame.

When using this product
  • keep out of eyes.  In case of contact with eyes, flush thoroughly with water
  • do not inhale or ingest
  • avoid contact with broken skin

Stop use and ask a doctor if
  • irritation and redness develop
  • 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 thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information
  • do not store above 105⁰F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, tocopheryl acetate, retinyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, mannitol, cellulose, hydroxypropyl methylcellulose, fragrance, yellow 5, blue 1, red 4, ultramarines

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds

Questions or comments? 1-800-910-6874
Dist. by Target Corp., Mpls., MN
Made in U.S.A. with U.S. and foreign components
Shop Target.com

Principal display panel

kills 99.99% of germs*

hand sanitizer kiwi punch

up & up

2 FL OZ (59.1 mL)

544.000/544AA

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-086
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL567 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
glycerin 
.ALPHA.-TOCOPHEROL ACETATE 
VITAMIN A PALMITATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
SULISOBENZONE 
MANNITOL 
POWDERED CELLULOSE 
HYPROMELLOSE 2208 (100 MPA.S) 
HYPROMELLOSES 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
FD&C RED NO. 4 
ULTRAMARINE BLUE 
Packaging
#Item CodePackage Description
1NDC:11673-086-1659 mL in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/14/2014
Labeler - Target Corp (006961700)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(11673-086)

 
Target Corp

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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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