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Hand Sanitizer by Unifirst First Aid Corporation

Medically reviewed on April 5, 2018

Dosage form: liquid
Ingredients: benzalkonium chloride 0.0039mg in 1mL
Labeler: Unifirst First Aid Corporation
NDC Code: 47682-522

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.

Henry Schein Hand Sanitizer
Drug Facts

Active Ingredient

Benzalkonium Chloride 0.39%

Purpose

Antiseptic

Uses:
  • for handwashing to decrease bacteria on the skin

Warnings:
  • For external use only
  • If swallowed seek medical attention
  • In case of contact with eyes, flush with water and contact a doctor
  • Discontinue use if skin irritation develops

Keep out of reach of children

Directions
  • Press pump twice to deliver foaming product into the palm of your hand
  • Rub hands together until hands are dry

Other information:
  • Store at 20° to 25 °C (68° to 77°)
  • May discolor certain fabrics

Inactive Ingredients

aloe vera, propylene glycol, fragrance, purified water, germaben II, ganex p-904 LC

Questions or Comments?

Call 1-800-634-7680

Principal Display Panel - Bottle Label

MEDI-FIRST®

Sani-Safe II

foaming hand sanitizer

  • alcohol-free
  • kills 99.9% of bacteria
  • dries instantly
  • contains aloe vera
  • non-irritating
  • 1.7 f. oz
HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-522
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (benzalkonium) benzalkonium chloride0.0039 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
aloe vera leaf 
propylene glycol 
diazolidinyl urea 
Packaging
#Item CodePackage Description
1NDC:47682-522-0150.269 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/09/2013
Labeler - Unifirst First Aid Corporation (832947092)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIOperations
Safetec of America, Inc.874965262MANUFACTURE(47682-522)

 
Unifirst First Aid Corporation

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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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