HAND SANITIZER- ethyl alcohol gel 
The Kroger Co

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Kroger Hand Sanitizer
396.000/396AA

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 fire or flame

when using this product

  • keep out of eyes.  In case 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, carbomer, fragrance, benzophenone-4, ext. violet 2, red 33

*EFFECTIVE AT ELIMINATNG 99.99% OF MANY COMMON HARMFUL GERMS AND ACTERIA IN AS LITTLE AS 15 SECONDS

DISTRIBUTED BY THE KROGER CO.,

CINCINNTI, OHIO 45202

QUALITY GUARANTEE

800-632-6900 - www.kroger.com

principal panel display

image description

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-941
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)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
SULISOBENZONE (UNII: 1W6L629B4K)  
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-941-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/08/201605/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)03/08/201605/07/2019
Labeler - The Kroger Co (006999528)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(30142-941)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(30142-941)

Revised: 4/2024
 
The Kroger Co