Your browser does not support JavaScript! CHLORHEXIDINE GLUCONATE SOLUTION [AURORA PHARMACEUTICAL LLC]

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CHLORHEXIDINE GLUCONATE solution
[Aurora Pharmaceutical LLC]


Category DEA Schedule Marketing Status
OTC ANIMAL DRUG LABEL unapproved drug other
NOTE: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.
Drug Label Sections

INDICATIONS

PRO-TEC™ ChlorSeptic 4% is a mild scrub containing chlorhexidine gluconate 4% that exhibits bactericidal activity against a wide range of microorganisms.

ACTIVE INGREDIENT

4% chlorhexidine gluconate.

OTHER INGREDIENTS

Purified water, lauramine oxide, isopropyl alcohol, polyethylene glycol, propanediol, hydroxyethylcellulose, aloe vera, fragrance and dye.

DIRECTIONS FOR USE

Wet area thoroughly with water. Pour approximately 5 mL of ChlorSeptic 4% and add enough water to make a lather. Lather thoroughly. Rinse thoroughly with clean water.

WARNINGS

Avoid contact with eyes and mucous membranes. If in eyes, immediately flush with water for 15 minutes and contact a physician. If swallowed, contact a physician and/or poison control center immediately.

For veterinary use only.

KEEP OUT OF REACH OF CHILDREN.

STORAGE

Store at 20°– 25° C (68°– 77° F). Excursions permitted between 15°– 30° C (59°– 86° F). Keep container tightly closed when not in use.

Take Time

REORDER NO: 59003

MANUFACTURED BY:
Aurora Pharmaceutical, LLC
NORTHFIELD, MINNESOTA 55057
888-215-1256
www.aurorapharmaceutical.com

IN 50-1149 REV 01

MANUFACTURED
IN THE USA

PRINCIPAL DISPLAY PANEL - 3.79 L Bottle Label

NDC 51072-047-01

PRO-TEC

CHLORSEPTIC
4%
with Aloe Vera

Antiseptic Antimicrobial
Skin Cleanser

Fast-acting, broad-spectrum
antimicrobial skin cleanser

For External Use Only

1 Gallon (3.79 L)

aurora
PHARMACEUTICAL®

PRINCIPAL DISPLAY PANEL - 3.79 L Bottle Label
CHLORHEXIDINE GLUCONATE 
chlorhexidine gluconate solution
Product Information
Product TypeOTC ANIMAL DRUG LABELItem Code (Source)NDC:51072-047
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Chlorhexidine Gluconate (Chlorhexidine) Chlorhexidine Gluconate40 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
Water786 g  in 1 L
ISOPROPYL ALCOHOL 
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) 
POLYETHYLENE GLYCOL 8000 
LAURAMINE OXIDE 
ACEMANNAN 
PROPANEDIOL 
FD&C GREEN NO. 3 
FD&C YELLOW NO. 5 
Product Characteristics
ColorGREENScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51072-047-014 in 1 CARTON
13.79 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER05/31/2012
Labeler - Aurora Pharmaceutical LLC (832848639)
Establishment
NameAddressID/FEIBusiness Operations
Aurora Pharmaceutical LLC832848639MANUFACTURE

Revised: 2/2013
 
Aurora Pharmaceutical LLC

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