Label: CHLORHEX 2X- chlorhexidine spray

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 15, 2012

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  • 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

    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 TypeOTC ANIMAL DRUGItem Code (Source)NDC:50989-918
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE40.000 g  in 1.0 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50989-918-240.240 L in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED DRUG OTHER10/11/2011
    Labeler - Vedco, Inc (021634266)
    Registrant - Continental Manufacturing Chemist, Inc. (005278007)
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