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Germ-X Advanced

Medically reviewed by Drugs.com. Last updated on May 11, 2020.

Dosage form: gel
Ingredients: ALCOHOL 700mg in 1mL
Labeler: Vi Jon, Inc
NDC Code: 11344-746

Germ-X  746.000/AA

claims

Introducting the most effective Germ-x formula ever

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

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses
  • to decrease bacteria on the skin that could cause disease
  • recommend for repeated use

Warnings

For external 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 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 hands thoroghly 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 105⁰ F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

Questions

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

Adverse reactions

Manufactured By: Vi-Jon, Inc. 

8515 Page Ave

St. Louis, MO 63114

www.germx.com

SDS MO-15036

SDA WI-2486

DSP-MO-28

DSP-MO-34

Pat.9,161,982

746.00/746AA

principal display panel

germ-X

ADVANCED

Hand Sanitizer

MORE EFFECTIVE FORMULA

kills more than 99.99% of germs

PATENTED

FORMULA

Original Scent

33.8 FL OZ (1 L)

GERM-X ADVANCED 
advanced hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-746
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
GLYCERYL CAPRYLATE/CAPRATE 
GLYCERIN 
ISOPROPYL MYRISTATE 
.ALPHA.-TOCOPHEROL ACETATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
SULISOBENZONE 
Packaging
#Item CodePackage Description
1NDC:11344-746-1659 mL in 1 BOTTLE, PLASTIC
2NDC:11344-746-34236 mL in 1 BOTTLE, PUMP
3NDC:11344-746-45946 mL in 1 BOTTLE, PLASTIC
4NDC:11344-746-26118 mL in 1 BOTTLE, PLASTIC
5NDC:11344-746-38295 mL in 1 BOTTLE, PLASTIC
6NDC:11344-746-32355 mL in 1 BOTTLE, PLASTIC
7NDC:11344-746-49443 mL in 1 BOTTLE, PLASTIC
8NDC:11344-746-881999 mL in 1 BOTTLE, PLASTIC
9NDC:11344-746-861000 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/21/2017
Labeler - Vi Jon, Inc (150931459)
Registrant - Vi-Jon, Inc. (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon, Inc.088520668manufacture(11344-746)

 
Vi Jon, Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.