Germ-X Advanced

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

Medically reviewed by Drugs.com. Last updated on May 1, 2023.

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11344-746
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	700 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
SULISOBENZONE

Packaging
#	Item Code	Package Description
1	NDC:11344-746-16	59 mL in 1 BOTTLE, PLASTIC
2	NDC:11344-746-34	236 mL in 1 BOTTLE, PUMP
3	NDC:11344-746-45	946 mL in 1 BOTTLE, PLASTIC
4	NDC:11344-746-26	118 mL in 1 BOTTLE, PLASTIC
5	NDC:11344-746-38	295 mL in 1 BOTTLE, PLASTIC
6	NDC:11344-746-32	355 mL in 1 BOTTLE, PLASTIC
7	NDC:11344-746-49	443 mL in 1 BOTTLE, PLASTIC
8	NDC:11344-746-88	1999 mL in 1 BOTTLE, PLASTIC
9	NDC:11344-746-86	1000 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/21/2017

Labeler - Vi Jon, Inc (150931459)

Registrant - Vi-Jon, Inc. (790752542)

Establishment
Name	Address	ID/FEI	Operations
Vi-Jon, Inc.		088520668	manufacture(11344-746)

Document Id: 26c45465-8bdb-4071-a717-79651a247ff5

Set id: 7e0b3300-6e22-41f8-8670-295d2ff213b3

Version: 3

Effective Time: 20200511

Vi Jon, Inc

Further information

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

Medical Disclaimer

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