HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Steris Corporation, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Uses

Healthcare Personnel Handwash to decrease bacteria on the skin before contact with patients under medical care or treatment

Warnings

For external use only-hands

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

skin irritation develops.  If condition persists more than 72 hours consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

• do not store above 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

benzophenone-4, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water

Questions or Comments

800-548-4873

adverse reaction section

Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds*

Soft' N Sure is a registered trademark of STERIS Corporation. Dignity Health and its logo are tradmarks of Dignity Health

Manufactured for:

STERIS Corporation

7501 Page Avenue

St. Louis, MO 63133 USA

800-548-4873   www.steris.com

951.001/951AB

principal display panel

NDC: 0519-8802-13

Dignity Health Hand Sanitizer Soft N SureAntiseptic Hand Gel

Moisturizing Fast Acting

8D02-26

For Hospital and Professional use Only

6542

8D02-XEA (F) (814)

NET CONTENTS: 444 mL (15 FL OZ)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0519-8802
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	578 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SULISOBENZONE (UNII: 1W6L629B4K)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
glycerin (UNII: PDC6A3C0OX)
isopropyl myristate (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0519-8802-13	444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014
2	NDC: 0519-8802-41	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/08/2014

Labeler - Steris Corporation (139424188)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(0519-8802)