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FOAMING HAND SANITIZER WITH ALOE

Medically reviewed on Jun 25, 2018

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.1000mL in 100mL
Labeler: APOLLO HEALTH AND BEAUTY CARE
NDC Code: 63148-240

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 BOX (BACK LABEL)

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE  0.1% (ANTISEPTIC)

USES AND DIRECTIONS
  • USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
  • DIRECTIONS: PUMP DESIRED AMOUNT ONTO HANDS AND RUB UNTIL YOUR SKIN IS DRY. CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

WARNINGS
  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT
  • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF
  • SKIN IRRITATION OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN
  • IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

PACKAGE FRONT AND BACK LABELS
  • 8OZ FRONT AND BACK LABELS: nc08.jpg
FOAMING HAND SANITIZER  WITH ALOE
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-240
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.1000 mL  in 100 mL
Packaging
#Item CodePackage Description
1NDC:63148-240-08236 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33306/25/2010
Labeler - APOLLO HEALTH AND BEAUTY CARE (201901209)

 
APOLLO HEALTH AND BEAUTY CARE

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Further information

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

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