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 2% 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 2% w/v Antiseptic 

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, Blue-1, Yellow-5, aloe vera, and other ingredients in a nonalkaline base.

Questions?

1-888-215-1256

REORDER NO: 59004

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

IN 50-1155 REV 01

MANUFACTURED IN THE USA

PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle Label

NDC 51072-048-01

PRO-TECTM

ChlorSeptic

2%

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 Type OTC ANIMAL DRUG Item Code (Source) NDC:51072-048
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 20 g  in 1 L
Product Characteristics
Color green Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51072-048-01 4 in 1 CARTON
1 3.79 L in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/31/2012
Labeler - Aurora Pharmaceutical LLC (832848639)

Revised: 10/2014
Document Id: bcfda1ff-1b93-452b-85c1-f7bc39d6eccc
Set id: 4035d9c5-778a-488b-8257-91d5cc3abd68
Version: 3
Effective Time: 20141022
 
Aurora Pharmaceutical LLC