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Germ-X

Dosage form: liquid
Ingredients: ALCOHOL 63mg in 1mL
Labeler: Vi Jon, Inc
NDC Code: 11344-234

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.

Drug Facts

claims

www.germx.com

Active ingredient

Ethyl Alcohol 63%

purpose

Antiseptic

Use
  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For exterenal use only-hands

Flammable

Keep away from heat and flame.

When using this product
  • keep out of eyes.  In case of contact with eyes, flush thoroghly 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 mre than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contract a Poison Control Cener 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

acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, fragrance, glycerin, tocopherol. water.

Questions

1-866 MY GERMX - 1-866-694-3769

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- 8515 Page Ave- St. Louis, MO 63114

Principal Display Panel

germ-X

HAND SANITIZER

KILLS 99.9% OF GERMS

MOISTRIZING

3 FL OZ (88 mL)

GERM-X 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-234
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL63 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) 
SULISOBENZONE 
GLYCERIN 
TOCOPHEROL 
WATER 
Packaging
#Item CodePackage Description
1NDC:11344-234-1659 mL in 1 BOTTLE, PLASTIC
2NDC:11344-234-1873 mL in 1 BOTTLE, PLASTIC
3NDC:11344-234-2189 mL in 1 BOTTLE, PLASTIC
4NDC:11344-234-34237 mL in 1 BOTTLE, PUMP
5NDC:11344-234-10295 mL in 1 BOTTLE, PUMP
6NDC:11344-234-40354 mL in 1 BOTTLE, PUMP
7NDC:11344-234-42828 mL in 1 BOTTLE, PUMP
8NDC:11344-234-83887 mL in 1 BOTTLE, PLASTIC
9NDC:11344-234-681656 mL in 1 BOTTLE, PLASTIC
10NDC:11344-234-2044 mL in 1 BOTTLE, PLASTIC
11NDC:11344-234-1659 mL in 1 BOTTLE, PLASTIC
12NDC:11344-234-49443 mL in 1 BOTTLE, PUMP
13NDC:11344-234-571182 mL in 1 BOTTLE, PUMP
14NDC:11344-234-881999 mL in 1 BOTTLE, PUMP
15NDC:11344-234-63199 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/12/1999
Labeler - Vi Jon, Inc (150931459)
Registrant - Vi Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi Jon150931459manufacture(11344-234)

Revised: 07/2015
 
Vi Jon, Inc

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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