ChlorHex 2X: Product Information

CHLORHEX 2X- chlorhexidine gluconate spray
Vedco, Inc

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 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:

Principle Panel
(click image for full-size original)

ChlorHex Spray

Distributed By

VEDCO, INC.

St. Joseph, MO 64507

Other Safety Information

TAKE TIME

OBSERVE LABEL DIRECTIONS

CHLORHEX 2X
chlorhexidine spray
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50989-918
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE) CHLORHEXIDINE GLUCONATE 40.000 g in 1.0 L
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50989-918-24 0.240 L in 1 BOTTLE, SPRAY None
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)

Revised: 06/2012 Vedco, Inc

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