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Hand Wash by DOLGENCORP,LLC

Medically reviewed on May 5, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: DOLGENCORP,LLC
NDC Code: 55910-085

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, lauramine oxide, PEG-150 distearate, sodium chloride, cetrimonium chloride, decyl glucoside, glycerin, fragrance, disteareth-75 IPDI, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, blue 1, red 33

Adverse reactions

DISTRIBUTED BY DOLGENCORP, LLC

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

100% SATISFATION GUARANTEED (888)309-9030

Package label

DG body

Antibacterial

Hand Soap

Spring

Rain

11.25 FL OZ (332 mL)

HAND WASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-085
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 
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 BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:55910-085-81332 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/10/2017
Labeler - DOLGENCORP,LLC (068331990)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(55910-085)

 
DOLGENCORP,LLC

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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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