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Hand Sanitizer by Vi-Jon

Medically reviewed on February 23, 2018

Dosage form: liquid
Ingredients: ALCOHOL .70mL in 1mL
Labeler: Vi-Jon
NDC Code: 11344-456

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.

Germ-X Advanced Foaming Hand Santizer

claims

germ-X

Professional

ADVANCED

FOAMING

HAND SANITIZER

Active ingredient

Ethyl alcohol 70%

purpose

Antiseptic

Use
  • 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 or redness develops
  • condition persists for more than 72 hours

Keep out of reach 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 suervision
  • 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, PEG-8 Dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, Isopropyl Myristate

claims

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

Adverse Reactions Section

DISTRIBUTED BY: VI-JON, INC.

8515 Page Ave

ST. LOUIS, MO 63114

vijonprofessional.com

456.001/456AC

principal display panel

germ-X

Professional

ADVANCED

FOAMING mm4.jpg

HAND SANITIZER

Kills 99.99% of Germs Instantly

Fragrance Free

Dye Free

128 FL OZ (1 GAL) 379 L

Principal Display Panel

germ-X

Professional

E3 ADVANCED FOAMING HAND SANITIZER

Kills 99.99% of Germs*

Fragrance & Dye Free

USDA

CERTIFIED

BIOBASED

PRODUCT

NSF

Nonfood Compounds Program Listed (Code E3)

7.5 FL OZ (221 mL)

HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-456
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL.70 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
PEG-8 DIMETHICONE 
MEADOWFOAMAMIDOPROPYL BETAINE 
GLYCERYL CAPRYLATE/CAPRATE 
GLYCERIN 
.ALPHA.-TOCOPHEROL ACETATE 
ISOPROPYL MYRISTATE 
Packaging
#Item CodePackage Description
1NDC:11344-456-451150 mL in 1 BOTTLE, PUMP
2NDC:11344-456-07750 mL in 1 BOTTLE, PLASTIC
3NDC:11344-456-1659 mL in 1 BOTTLE, PLASTIC
4NDC:11344-456-96221 mL in 1 BOTTLE, PLASTIC
5NDC:11344-456-49443 mL in 1 BOTTLE, PLASTIC
6NDC:11344-456-43473 mL in 1 BOTTLE, PLASTIC
7NDC:11344-456-44532 mL in 1 BOTTLE, PLASTIC
8NDC:11344-456-861000 mL in 1 BOTTLE, PLASTIC
9NDC:11344-456-083785 mL in 1 BOTTLE, PLASTIC
10NDC:11344-456-2044 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/10/2016
Labeler - Vi-Jon (150931459)
Registrant - Vi-Jon, Inc (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon, Inc150931459manufacture(11344-456)

 
Vi-Jon

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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