HAND SANITIZER- ethyl alcohol gel 
Walgreens

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 469.000  469AA

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Uses

Warnings

For external use only: hands

Flammable

Keep away from heat and flame

when using this product

Stop use and ask a doctor

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, carbomer, fragrance, benzophenone-4, mannitol, cellulose, hydroxypropyl methylcellulose, ultamarines

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

Walgreens

Hand

Sanitizer

Coconut

water scent

2 FL OZ (59 mL)

image description

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0469
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL545 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)  
CELLULOSE ACETATE (UNII: 3J2P07GVB6)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
ULTRAMARINE BLUE (UNII: I39WR998BI)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0469-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/26/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/26/2015
Labeler - Walgreens (008965063)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(0363-0469)

Revised: 6/2022
Document Id: c99a3528-3766-4f29-b806-f3fe410450d0
Set id: 54ee7d47-af91-4360-9f0f-4a1bde12199c
Version: 14
Effective Time: 20220610
 
Walgreens