HAND SANITIZING WIPES- ethyl alcohol cloth

Hand Sanitizing Wipes by

Drug Labeling and Warnings

Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, Vi-jon, Israel. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

to decrease bacteria on the skin

Warings

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

In case of accidental ingestion, see professional assistance or contact a Poison Control Center immediately.

Directions

• wipe hands thoroughly with product and allow to dry
• for children under 6, use only under adult supervison
• not recommended for infants

Inactive ingredients

aloe barbadensis extract, fragrance, glycerin, lactic acid, 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

Made in Israel

Distributed by 

Vi-Jon

8515 Page Ave.

St. Louis MO 63114

231.001/231AB

principal display panel

germ-X

moisturizing

Hand Sanitizing

KILLS 99.99% OF GERMS

100 individually wrapped wipes

6 in x 8 in (15.24 CM x 20.32 CM)

INGREDIENTS AND APPEARANCE

HAND SANITIZING WIPES 
ethyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-231
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
LACTIC ACID (UNII: 33X04XA5AT)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-231-93	100 in 1 BOX	01/05/2009
1		3.0 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/05/2009

Labeler - Vi-Jon (150931459)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-jon		150931459	manufacture(11344-231)

Establishment
Name	Address	ID/FEI	Business Operations
Israel		143406457	manufacture(11344-231)