ANTIBACTERIAL HAND WASH- ethyl alcohol liquid 
Vi-Jon, Inc

----------

Germ-X everywhere Moisturizing Hand Sanitizer
467

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Uses

  • to decrese 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 or redness develops
  • 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 hand 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 105°F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, acrylates/C10-30 alkyl crosspolymer, tocopheryl acetate, benzophenone-4

DISTRIBUTED BY: VI-JON, INC.

ST. LOUIS, MO 63114

467.000/467AA

principal display

germ-x everywhere

FRAGRANCE FREE MOISTURIZING HAND SANITIZER

1150 mL (39 FL OZ)

image description

ANTIBACTERIAL HAND WASH 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-467
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol1.313 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
SULISOBENZONE (UNII: 1W6L629B4K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11344-467-04750 mL in 1 POUCH; Type 0: Not a Combination Product07/28/201610/18/2018
2NDC:11344-467-451150 mL in 1 POUCH; Type 0: Not a Combination Product07/28/201610/18/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)07/28/201610/18/2018
Labeler - Vi-Jon, Inc (088520668)
Registrant - Vi-Jon, Inc (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon. nc088520668manufacture(11344-467)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon. nc790752542manufacture(11344-467)

Revised: 11/2023
 
Vi-Jon, Inc