INFECTIGUARD HAND SANITIZER- ethyl alcohol gel

Infectiguard Hand Sanitizer by

Drug Labeling and Warnings

Infectiguard Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dr. Fresh, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For handwashing to decrease bacteria on the skin.

Warnings

Flammable, keep away from fire or flame. For external use only.

When using this product

For external use on hands only. In case of contact with eyes, rinse with water.

Stop use and ask a doctor

if irritation and redness develops or persists

Keep out of reach of children

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

Directions

Wet hands with product and rub briskly until dry.

Other Information

Do not store above 100F May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive Ingredients

Water, Carbomer, Fragrance, Triethanolamine, Glycerin, Propylene Glycol, Isopropyl Alcohol, Isopropyl Myristate, Vitamin E, Aloe Vera Extract

SPL UNCLASSIFIED SECTION

Infectiguard and related trademarks, names, logos, and patents are the property of Dr. Fresh. Inc. and are registered and/or used in the U.S. and countries around the world Dr. Fresh, Inc.

100% Satisfaction Guaranteed

Dr. Fresh

Distributed by:

USA Dr. Fresh, Inc.
Buena Park, CA 90620
Canada - Dr. Fresh, Inc.
Ontario, Canada L7C2T4
U.K. - Grosvenor Consumer Products Limited

(Dr. Fresh, UK)
268 Bath Road, Slough
Berkshire SL1 4DX, UK

Questions? Comments?

Toll-Free: 1-866-3737374
USA: 714-690-1573
UK and IRL: +44-(0)1753725365
comments@drfresh.com

visit us online at:
www.drfresh.com
www.drfresh.co.uk
Made in PRC

Product Labeling

infectiguard

Instant Hand Sanitizer

Moisturizing with Vitamin E and Aloe

Kills Germs, Not your hands

Kills 99.99% of harmful germs
Moisturizing

12fl oz
(355ml)

INGREDIENTS AND APPEARANCE

INFECTIGUARD HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64893-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64893-030-12	355 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/27/2012

Labeler - Dr. Fresh, Inc. (033059119)