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Sport Mate Non-Alcohol Foaming Instant Hand Sanitizer

Dosage form: solution
Ingredients: benzalkonium chloride 1g in 1000mL
Labeler: Stone Soap Company, Inc.
NDC Code: 62065-514

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 0.1%



  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use


For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if 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.

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry

Inactive Ingredients

Water, dihydroxpropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Principal Display Panel

Sport Mate

Non-Alcohol Foaming Instant Hand Sanitizer

  • Enhanced with Moisturizers
  • Kills disease causing germs within seconds
  • Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
  • Assists with OSHA Bloodborne Pathogen Standard Compliance

See side panel for additional information.

For Hospital and Professional Use Only

husky 514 solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62065-514
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (benzalkonium) benzalkonium chloride1 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
dihydroxypropyl PEG-5 linoleammonium chloride 
glycereth-2 cocoate 
behentrimonium chloride 
dihydroxyethyl cocamine oxide 
#Item CodePackage Description
1NDC:62065-514-521893 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33303/21/2010
Labeler - Stone Soap Company, Inc. (005365119)
Registrant - Stone Soap Company, Inc. (005365119)
Canberra Corporation068080621MANUFACTURE

Stone Soap Company, Inc.

Medically reviewed on Apr 2, 2018

Further information

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