HAND WASH- benzalkonium chloride liquid 
Target Corporation

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.

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UP & Up 358

Active ingredient

Benzalkonium chloride 0.10%

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, glycerin, cetrimonium chloride, cocamide MEA, lauramidopropylamine oxide, myristamidopropylamine oxide, PEG-120 methyl glucose dioleate, fragrance, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, green 3, yellow 10

claims

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

Adverse reactions

Distributed by Target Corporation, Mpls., MN 55403

2017 Target Brands, Inc.

principal display panel

antibacterial

foaming hand wash

pear scent

helps fight

germs

up & up

40 FL OZ (1.18 L)

image description

HAND WASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-358
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.999 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-358-96222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/201404/29/2021
2NDC:11673-358-031478 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/201404/29/2021
3NDC:11673-358-571182 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/201404/29/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/201404/29/2021
Labeler - Target Corporation (006961700)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(11673-358)

Revised: 4/2021
 
Target Corporation