CHLORHEX 2X- chlorhexidine spray

ChlorHex 2X by

Drug Labeling and Warnings

ChlorHex 2X by is a Animal medication manufactured, distributed, or labeled by Vedco, Inc, Continental Manufacturing Chemist, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Indications:

For Mild to severe dermatological conditions where a full strength antiseptic, antimicrobial and deodorizing formulation may be of benefit.

Precautions:

 For topical use only on Dogs, Cats and Horses.  Avoid contact with eyes.  If irritation develops, discontinue use and consult your veterinarian.

Storage

 Store product at room temperature.

Active Ingredient:

 Chlorhexidine Gluconate 4%

Inactive Ingredients:

 Allantoin, Aloe Vera Gel, FD&C Blue #1, Fragrance, Isopropyl Alcohol, Polysorbate, Purified Water

Directions for Use:

 Shake well before each use.  Spray directly onto the affected area(s) 2-3 times daily, or as directed by veterinarian.  Distract animal for several minutes following treatment to prevent licking.

Product Description

 ChlorHex 2X 4% Spray is a maximum strength antimicrobial spray containing penetrating agents, allantoin and aloe vera for optimal thera peutic effectiveness.

Keep Out of Reach of Children

For Use on Dogs, Cats and Horses

For Animal Use Only

Package Label

 Label for 8oz product:

ChlorHex Spray

Distributed By

 VEDCO, INC.

St. Joseph, MO 64507

Other Safety Information

 TAKE TIME

OBSERVE LABEL DIRECTIONS

INGREDIENTS AND APPEARANCE

CHLORHEX 2X 
chlorhexidine spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 50989-918
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	40.000 g  in 1.0 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50989-918-24	0.240 L in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		10/11/2011

Labeler - Vedco, Inc (021634266)

Registrant - Continental Manufacturing Chemist, Inc. (005278007)