GERM-X ADVANCED- advanced hand sanitizer gel

Germ-X Advanced by

Drug Labeling and Warnings

Germ-X Advanced by is a Otc medication manufactured, distributed, or labeled by Vi Jon, LLC, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

GERM-X ADVANCED 
advanced hand sanitizer gel

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
SULISOBENZONE (UNII: 1W6L629B4K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-746-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
2	NDC: 11344-746-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/21/2017
3	NDC: 11344-746-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
4	NDC: 11344-746-26	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
5	NDC: 11344-746-38	295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
6	NDC: 11344-746-32	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
7	NDC: 11344-746-49	443 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
8	NDC: 11344-746-88	1999 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/21/2017
9	NDC: 11344-746-86	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/21/2017

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	Business Operations
Vi-Jon, Inc.		088520668	manufacture(11344-746)