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Hand Sanitizer by Steris Corporation

Dosage form: gel
Ingredients: ALCOHOL 578mg in 1mL
Labeler: Steris Corporation
NDC Code: 0519-8802

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Soft n Sure Hand Sanitizer

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

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

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)

951.001/951AA/AB

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0519-8802
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL578 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SULISOBENZONE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
glycerin 
isopropyl myristate 
PROPYLENE GLYCOL 
.ALPHA.-TOCOPHEROL ACETATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:0519-8802-13444 mL in 1 BOTTLE, PLASTIC
2NDC:0519-8802-411000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/08/2014
Labeler - Steris Corporation (139424188)
Registrant - Vi-Jon (088520668)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(0519-8802)

 
Steris Corporation

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Medically reviewed on Aug 14, 2017

Further information

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

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