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Clorox Hand Sanitizer

Dosage form: solution
Ingredients: ALCOHOL 71mL in 100mL
Labeler: The Clorox Company
NDC Code: 26509-0106

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.

Active Ingredient

Alcohol 71% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help decrease bacteria on skin that can potentially cause disease.

Warnings

Flammable. Keep away from fire or flame.

For external use only.

Do not use in the eyes.

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 immediately.

DIrections
  • Spray on clean, dry hands and nails
  • Wet hands thoroughly with product
  • Rub hands together for no less than 15 seconds, paying particular attention to interdigital spaces, fingernails and cuticles
  • Allow to dry without wiping
  • Rub hands together briskly until dry

Other Information
  • Store in a cool, dry place below 104 deg F (40 C)

Inactive Ingredients

Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate

Questions or Comments?

Viisit us at www.cloroxprofessional.com or call 1-888-797-7225.

Clorox Hand Sanitizer

CLOROX HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0106
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL71 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERYL LAURATE 
GLYCERIN 
ISOPROPYL ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:26509-0106-159 mL in 1 BOTTLE, SPRAY
2NDC:26509-0106-4500 mL in 1 BOTTLE, SPRAY
3NDC:26509-0106-51000 mL in 1 BOTTLE
4NDC:26509-0106-61000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/06/2006
Labeler - The Clorox Company (009138033)

 
The Clorox Company

Medically reviewed on Oct 16, 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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