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Clorox Care Concepts Antimicrobial

Medically reviewed on November 14, 2017

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE .12g in 100mL
Labeler: The Clorox Company
NDC Code: 26509-0003

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 0.12%

Purpose

Antiseptic handwash

Use
  • For handwashing to decrease bacteria on skin that potentially can cause disease
  • Recommended for repeated use

Warnings

For external use only.

When using this product, do not use in the eyes.

Discontinue use and ask a doctor if

  • irritate 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
  • Wet hands and forearms.
  • Dispense onto hands.
  • Scrub thoroughly for 30 seconds.
  • Rinse and repeat.

Inactive ingredients

Benzyl Alcohol, Citric Acid, Cocamidopropyl Betaine, Dehydroacetic Acid, Glycerin, Phenoxyethanol, Poloxamer 124, Sodium Hydroxide, Tetra Sodium EDTA, Water

Clorox Care Concepts

Antimicrobial Soap

CLOROX CARE CONCEPTS ANTIMICROBIAL 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0003
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE.12 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL 
CITRIC ACID MONOHYDRATE 
COCAMIDOPROPYL BETAINE 
DEHYDROACETIC ACID 
GLYCERIN 
PHENOXYETHANOL 
POLOXAMER 124 
SODIUM HYDROXIDE 
EDETATE SODIUM 
WATER 
Packaging
#Item CodePackage Description
1NDC:26509-0003-144 mL in 1 BOTTLE, PUMP
2NDC:26509-0003-2249 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/07/2014
Labeler - The Clorox Company (009138033)
Registrant - The Clorox Company (009138033)

 
The Clorox Company

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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