HAND SANITIZER- ethyl alcohol gel 
Walgreen Co

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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Hand Sanitizer
646

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

Warnings

For external use only: hands

Flammable, keep away from fire or 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, carbomer, fragrance, hydroxypropyl methylcellulose, retinyl palmitate, tocopheryl acetate, mannitol, cellulose, ultramarines, yellow 5, blue 1

*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, IL 60015

100% Satisfaction Guaranteed

walgreens.com (c)2015 Walgreen Co.

principal display panel

Well at Walgreens

Hand Sanitizer

Fresh pear scent

KILLS 99.99% OF GERMS*

2 FL OZ (59 mL)

image description

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0643
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL558 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
glycerin (UNII: PDC6A3C0OX)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
MANNITOL (UNII: 3OWL53L36A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
ULTRAMARINE BLUE (UNII: I39WR998BI)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0643-0659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/10/2016
Labeler - Walgreen Co (008965063)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(0363-0643)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(0363-0643)

Revised: 8/2022
Document Id: b71aa141-86c1-4667-a0e2-2ce8a8c4c1bb
Set id: b746c9a6-8fd8-42f6-ab63-18316b0fe925
Version: 9
Effective Time: 20220809
 
Walgreen Co