CHLORHEXIDINE GLUCONATE- chlorhexidine gluconate 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.

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ChlorSeptic 4% with Aloe Vera

ChlorSeptic continues to kill germs up to 6 hours after washing, is gentle to skin, and prevents skin infections, thereby reducing the risk of cross-infection.

DRUG FACTS

 ACTIVE INGREDIENT PURPOSE
 Chlorhexidine Gluconate 4% w/vAntiseptic 

USES

WARNINGS

For external use only

Do not use

When using this product

Stop use and ask a doctor if irritation, sensitization or allergic reaction occurs and lasts for 72 hours. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

Other information

Store between 20°–25° C (68°–77° F).

Inactive Ingredients

Fragrance, isopropyl alcohol 4% w/v, purified water, Red 40, aloe vera, and other ingredients in a nonalkaline base.

Questions?

1-888-215-1256

REORDER NO: 59003

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

IN 50-1149 REV 00

MANUFACTURED IN THE USA

PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle Label

NDC 51072-047-01

PRO-TEC´╗┐TM

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 - 1 Gallon 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
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
2NDC:51072-047-080.237 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)

Revised: 10/2014
Document Id: 19e70711-c3ce-436c-a282-2a4403275f93
Set id: 01213b4e-477a-49d3-83b2-dadff4f1cb7d
Version: 3
Effective Time: 20141022
 
Aurora Pharmaceutical LLC