ADVANCED HAND SANITIZER- ethyl alcohol gel 
The Kroger 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.

----------

Krogers Advanced Hand Sanitizer with Aloe
439.001/439AC rev 1

Active ingredient

Ethyl alcohol 70%

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 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, aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

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

DISTRIBUTED BY: THE KROGER CO., CINCINNATI, OHIO 45202

QUALITY GUARANTEE

800-632-6900 www.kroger.com

principal display panel

Kroger

ALOE VERA

HAND SANITIZER

KILLS 99.99% OF GERMS*

32 FL OZ (946 mL)

image description

ADVANCED HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-439
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
SULISOBENZONE (UNII: 1W6L629B4K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-439-34236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/15/2013
2NDC:30142-439-38295 mL in 1 PACKAGE; Type 0: Not a Combination Product01/15/2013
3NDC:30142-439-45946 mL in 1 PACKAGE; Type 0: Not a Combination Product01/15/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/15/2013
Labeler - The Kroger CO. (006999528)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(30142-439)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(30142-439)

Revised: 3/2022
Document Id: b969c7aa-1f34-4821-b3b1-e6fd5c121293
Set id: bcae0067-2ee5-4734-a343-ce1327bffe6c
Version: 10
Effective Time: 20220302
 
The Kroger CO.