Label: CHLORHEXIDINE GLUCONATE solution

  • NDC Code(s): 51072-048-01
  • Packager: Aurora Pharmaceutical, Inc.
  • Category: OTC ANIMAL DRUG LABEL

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Drug Label Information

Updated February 23, 2023

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  • INDICATIONS

    PRO-TEC® ChlorSeptic 2% is a mild scrub containing chlorhexidine gluconate 2% that exhibits bactericidal activity against a wide range of microorganisms.

  • ACTIVE INGREDIENT

    2% chlorhexidine gluconate

  • DIRECTIONS FOR USE

    Wet area thoroughly with water. Pour approximately 5 mL of ChlorSeptic 2% and add enough water to make a lather. Lather thoroughly. Rinse thoroughly with clean water.

  • WARNINGS

    Avoid contact with eyes and mucous membranes. If in eyes, immediately flush with water for 15 minutes and contact a physician. If swallowed, contact a physician and/or poison control center immediately.

    Do not use if allergic or sensitive to the active ingredients.

    For veterinary use only.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • STORAGE

    Store upright at 20°–25° C (68°–77° F). Excursions permitted between 15°-30° C (59°-86° F). Keep container tightly closed when not in use. Do not freeze.

  • OTHER INGREDIENTS

    Fragrance, isopropyl alcohol, water, dye, aloe vera and other ingredients in a nonalkaline base.

  • SPL UNCLASSIFIED SECTION

    take time image

    MANUFACTURED IN THE USA

    REORDER NO: 59004

    MANUFACTURED BY:
    Aurora Pharmaceutical, Inc.
    NORTHFIELD, MINNESOTA 55057
    1-888-215-1256
    www.aurorapharmaceutical.com

    IN 50-1155  02/2021

  • PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle Label

    NDC 51072-048-01

    PRO-TEC®

    ChlorSeptic

    2%

    with Aloe Vera

    Antiseptic Antimicrobial Skin Cleanser

    Fast-acting, broad-spectrum antimicrobial skin cleanser

    For External Animal Use Only

    1 Gallon (3.79 L)

    AURORA PHARMACEUTICAL®

    PRINCIPAL DISPLAY PANEL - 1 Gallon Bottle Label

  • INGREDIENTS AND APPEARANCE
    CHLORHEXIDINE GLUCONATE 
    chlorhexidine gluconate solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51072-048
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE20 g  in 1 L
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51072-048-014 in 1 CARTON
    13.79 L in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/31/2012
    Labeler - Aurora Pharmaceutical, Inc. (832848639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurora Pharmaceutical, Inc.832848639manufacture
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