HAND SANITIZER- ethyl alcohol gel 
Walgreen

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.

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Walgreens Hand Sanitizer
544.000/544AA

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Use

Warnings

For external use only: hands

Flammable.  Keep away from heat and flame.

when using this product

Stop use and ask a doctor if

Keep  out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

water, glycerin, tocopheryl acetate, retinyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, mannitol, cellulose, hydroxypropyl methylcellulose, fragrance, yellow 5, blue 1, red 4, ultramarines

*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

DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL60015
100% satisfaction guaranteed
walgreens.com

principal display panel

Well at Walgreens

NEW

Hand Sanitizer Guava fruit

scent

2 FL OZ (59 mL)

image description

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0898
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL567 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
glycerin (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
SULISOBENZONE (UNII: 1W6L629B4K)  
MANNITOL (UNII: 3OWL53L36A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
ULTRAMARINE BLUE (UNII: I39WR998BI)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0898-1659 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product04/04/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/04/2016
Labeler - Walgreen (008965063)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(0363-0898)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(0363-0898)

Revised: 3/2022
Document Id: afcb1c69-5580-4cf8-b31d-1d859f9e6c58
Set id: 6a61abf8-77e4-42e5-bd58-c046fe227633
Version: 9
Effective Time: 20220307
 
Walgreen