Label: T-HEXX DRY TEAT DIP- povidone solution

  • 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 September 19, 2023

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

  • SPL UNCLASSIFIED SECTION

    T-HEXX®
    Animal Health
    External Teat Dip DRY™

  • INACTIVE INGREDIENT

    Ingredients:

    Ethanol, Ethyl Acetate, Water, Acid Blue 9, Polyvinylpyrrolidone

  • SPL UNCLASSIFIED SECTION

    Net Contents: 0.95 liters (32 fl. oz.)

    Teat protection dip for dry cows.

  • INDICATIONS & USAGE

    For Dry Cows
    T-Hexx DRY Teat Dip is a safe and easy to use dry cow teat dip that uses patented technology to safely and effectively seal
    and protect the teats at dry off in your program producing a physical barrier to aid in reducing the spread of organisms
    which may cause mastitis.

    Directions For Use
    Use in a well ventilated area. Do not pour ununused product back into original container. Keep container tightly closed when
    not in use. Apply with a disposable paper cup.

    At Dry Off
    At last milking prior to dry off, milk out cow completely. Clean and dry teats, then dip entire length of teat with T-HEXX DRY
    Teat Dip. For maximum protection, a second application may be applied after the first coating is dry.

    10 Days Prior to Calving
    Clean teat throughly and wipe with dry towel. Dip entire length of teat into T-HEXX DRY Teat Dip. Dip should remain on teat
    3-7 days. Observe daily and re-dip if product is removed prior to calving. After calving, peel off any remaining teat dip prior
    to milking.

  • USER SAFETY WARNINGS

    NOT FOR HUMAN USE
    For External Use Only
    READ THIS LABEL AND THE SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
    KEEP OUT OF REACH OF CHILDREN

    GHS Symbols

    Danger:
    Highly flammable liquid and vapour. Causes serious eye irritation.
    Caution: Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Keep container tightly closed.
    Ground/Bond container and receiving equipment. Use explosion-proof electrical/ventilating/lighting equipment. Use only non-sparking
    tools. Take precautionary measures against static discharge. Wash hands, forearms and face thoroughly after handling. Wear protective
    gloves/protective clothing/eye protection/face protection. FIRST AID: Skin/Hair: Take off immediately all contaminated clothing. Rinse
    skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do.
    Continue rinsing. If eye irritation persists: Get medical advice/attention. In case of fire: Use media other than water to extinguish. Store
    in a well-ventilated place. Keep cool. Dispose of contents/container to hazardous or special waste collection point, in accordance with
    local, regional, national and/or international regulation.

  • SPL UNCLASSIFIED SECTION

    Lot and expiry on bottom of package.

    T-HEXX is a trademark of Huvepharma Inc.

    US Patents 6,203,812, 6,395,289, 6,440,442 and other Patents Pending

    Manufactured in the USA for Huvepharma Inc.

    20927 State Route K, St. Joseph, MO 64505, 800-542-8916

  • PRINCIPAL DISPLAY PANEL

    Front Label

    Back Label

  • INGREDIENTS AND APPEARANCE
    T-HEXX DRY TEAT DIP 
    povidone solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:23243-8505
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE.910 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    ETHYL ACETATE (UNII: 76845O8NMZ)  
    ACID BLUE 9 AMMONIUM (UNII: 86R7G3C26F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:23243-8505-50.95 L in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/22/2023
    Labeler - Huvepharma, Inc (619153559)