Label: OXIPRO- 1% hydrogen peroxide teat dip solution

  • NDC Code(s): 60648-9010-1, 60648-9010-2, 60648-9010-3, 60648-9010-4, view more
    60648-9010-5, 60648-9010-6, 60648-9010-7
  • Packager: Preserve International
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated May 17, 2019

If you are a consumer or patient please visit this version.

  • DOSAGE & ADMINISTRATION

    OXIPRO is a 1% hydrogen Peroxide and Sodium Lactate teat dip.​

    APPLICATION:

    Recommended for both pre and post dipping applications.

    FOR PRE-DIPPING: Make sure udder and teats are visibly clean of any soil.  Dip with OXIPRO solution.  Forestrip and wipe teat with towel and then attach milking unit.

    FOR POST-DIPPING: Dip Entire teat in OXIPRO.Allow to air dry.  If solution in cup becomes visibly dirty or cloudy, then replenish with OXIPRO at full strength.  Do not return unused product to original container.

    DO NOT MIX OXIPRO WITH ANY OTHER TEAT SPRAY OR DIP OR OTHER PRODUCTS.

    NOTE:

    OXIPRO is not intended to cure or help the healing of chapped or irritated teats.  In case of teat irritation or chapping, have the condition examined.

    This product does not contain NPE (Nonylphenol Ethoxylate) Surfactant.

    PROTECT FROM FREEZING

    IF FROZEN:  SHAKE VIGOROUSLY AFTER THAWING

    TAKE TIME  OBSERVE LABEL DIRECTIONS

  • WARNING:

    CONTAINS HYDROGEN PEROXIDE SOLUTION

    Avoid contamination of food.  Avoid contact with eyes.  Not for internal use. Not for human use.

    KEEP OUT OF REACH OF CHILDREN

    DO NOT GET IN EYES OR ON CLOTHING

    HARMFUL IF SWALLOWED

    FIRST AID:

    INHALATION: No irritation expected.  Move the exposed person to fresh air.

    EYE​ CONTACT​:​  Rinse immediately with plenty of water.  Contact lenses should be removed.

    ​SKIN CONTACT:​  No irritation expected.  Rinse immediately with plenty of water.

    ​INGESTION:​ DO NOT INDUCE VOMITING unless advised to do so by a doctor.  Never give anything by mouth to an unconscious person.

    GET MEDICAL ATTENTION IMMEDIATELY.

    ​FOR PRODUCT EMERGENCY CONTACT:  Chem-Tel Inc. 1-800-255-3924

    HAZARD STATEMENTS:

    May intensify fire; oxidizer.

    PRECAUSTIONARY STATEMENTS:

    P210 - Keep away from heat, hot surfaces, sparks, open flames and other ignition sources.  No smoking.

    P220 - Keep/Store away from clothing/combustible materials.

    P221 - Take any precaution to avoid mixing with combustibles.

    P280 - Wear protective gloves/protective clothing/eye protection/face protection.

  • PRINCIPAL DISPLAY PANEL

    OXIPRO

    HYDROGEN PEROXIDE TEAT DIP

    Active Ingredients:

    Active Hydrogen Peroxide..........1.00%
    pH.....................................Minimum 4.75
    Contains a 10% Glycerin and Anionic Surfactants

    Oxipro

    Manufactured By: Preserve International​®

    Preserve International​®​ is a wholly-owned subsidiary of Neogen​®​ Corporation.

    NEOGEN​®

    944 Nandino Blvd.

    Lexington, KY  40511

    859-254-1221 or 800-621-8829

    animalsafety.neogen.com

  • INGREDIENTS AND APPEARANCE
    OXIPRO 
    1% hydrogen peroxide teat dip solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:60648-9010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE11.03 g  in 1 L
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN102.75 g  in 1 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60648-9010-13.78 L in 1 JUG
    2NDC:60648-9010-218.9 L in 1 PAIL
    3NDC:60648-9010-356.7 L in 1 DRUM
    4NDC:60648-9010-4113.4 L in 1 DRUM
    5NDC:60648-9010-5207.9 L in 1 DRUM
    6NDC:60648-9010-6945 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
    7NDC:60648-9010-71039.5 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/18/2019
    Labeler - Preserve International (808154199)