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Hand Sanitizer by Walgreen Co

Medically reviewed on March 26, 2018

Dosage form: gel
Ingredients: ALCOHOL 567mg in 1mL
Labeler: Walgreen Co
NDC Code: 0363-0596

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

Ethyl alcohol 63%

Purpose

Antiseptic

Uses
  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only: hands

Flammable

Keep away from heat and flame

when using this product
  • keep out of eyes.  Incase of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest

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 right away

Directions
  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information
  • do not store above 105⁰F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, tocopheryl acetate, retinyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, mannitol, cellulose, hydroxypropyl methylcellulose, fragrance, ext. violet 2, blue 1, red 40, ultramarines

claims

Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds

Questions or Comments? 1-800-925-4733

adverse reactions section

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

walgreens.com

MADE IN U.S.A. WITH US AND FOREIGN COMPONENTS

Principal display panel

Well at

Walgreens

NEW

Hand

Sanitizer

Coastal

Breeze Scent

Kills 99.99% of germs

2 FL OZ (59 mL)

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0596
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL567 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
glycerin 
.ALPHA.-TOCOPHEROL ACETATE 
VITAMIN A PALMITATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
SULISOBENZONE 
MANNITOL 
POWDERED CELLULOSE 
HYPROMELLOSES 
EXT. D&C VIOLET NO. 2 
FD&C BLUE NO. 1 
FD&C RED NO. 40 
ULTRAMARINE BLUE 
Packaging
#Item CodePackage Description
1NDC:0363-0596-1659 mL in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/26/2015
Labeler - Walgreen Co (008965063)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(0363-0596)

 
Walgreen Co

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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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