BARRIER WATERLESS SURGICAL PREP - povidone-iodine, alcohol and isopropyl alcohol solution 
Aurora Pharmaceutical LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

INDICATIONS

For use in cattle, sheep and
swine as an aid in reducing surface bacteria.
Barrier™ Waterless Surgical Prep provides
rapid antimicrobial kill of a broad spectrum of
microorganisms, including antibiotic-resistant
strains, with greater than 99% microbial kill
in 15 seconds or less.

Closely clip hair from surgical
site. Hold sprayer about 4–6 inches from
area to be treated. Spray 1 or more times
— allow to dry. Surgical incision can then
be made through the durable antibacterial
Barrier™ protection.

Do not use in
the eyes. Do not use if you
are allergic to povidone-iodine.
Prolonged exposure may cause
irritation. If swallowed, get
medical help or contact a Poison
Control Center right away.

Store at 15°–30° C (59°–86° F)

Manufactured by:
Aurora Pharmaceutical, LLC
Northfield, Minnesota 55057

NDC 51072-035-16

BARRIER

Waterless Surgical Prep
Povidone-Iodine
2% Available Iodine

For Veterinary Use Only
16 fl. oz. (473 ml)

PRINCIPAL DISPLAY PANEL - 473 ml Bottle Label




BARRIER  WATERLESS SURGICAL PREP
povidone-iodine, alcohol, isopropyl alcohol solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51072-035
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (POVIDONE-IODINE) POVIDONE-IODINE20 g  in 100 mL
ALCOHOL (ALCOHOL) ALCOHOL63.8 g  in 100 mL
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL3.4 g  in 100 mL
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEFRUIT (GRAPEFRUIT GINGER) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMultilevel Packaging
1NDC:51072-035-16473.2 mL in 1 BOTTLE, SPRAYNone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/20/2010

Labeler - Aurora Pharmaceutical LLC (832848639)
Establishment
NameAddressID/FEIOperations
Aurora Pharmaceutical LLC832848639manufacture
Establishment
NameAddressID/FEIOperations
BASF Corporation623867848api manufacture

Revised: 11/2011 Aurora Pharmaceutical LLC