Label: BOVAPRO 110- iodine solution solution

  • NDC Code(s): 17307-3202-1, 17307-3202-2, 17307-3202-3, 17307-3202-4
  • Packager: AgroChem USA, LLC
  • 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 October 14, 2024

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

  • DESCRIPTION

    BovaPro 110

  • SPL UNCLASSIFIED SECTION

    TEAT DIP

  • WARNINGS

    WARNING

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS AND PRECAUTIONS

    NOT FOR HUMAN USE.

    AVOID FREEZING.

    KEEP OUT OF DIRECT SUNLIGHT.

    CAUSES SERIOUS EYE IRRITATION.

    FOR FARM AND INDUSTRIAL USE ONLY.

    PREVENTION:  Wash skin thoroughly after handling. Wear eye protection/ face protection.

    FIRST AID / RESPONSE: 

    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.          

  • STORAGE AND HANDLING

    STORAGE:  Store locked up.                       

    DISPOSAL: Dispose of contents/ container to an approved waste disposal plant .

  • SPL UNCLASSIFIED SECTION

    EMERGENCY TELEPHONE NUMBER (Chemtrec) 800-424-9300 CCN205494

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT: Iodine 1.0 % (10% Polyethoxy Polypropoxy Polyethoxy Ethanol - Iodine Complex) Titration via USP33 Reissue, Topical Solution

  • INACTIVE INGREDIENT

    EMOLLIENTS:  10.0%  

  • SPL UNCLASSIFIED SECTION

    BovaPro  110  is  made  with  IoPlex  technology  and  is  NPE  free.

    NET CONTENTS:  55 GALLON (208.2L)

    LOT:

    EXP. DATE:

    Use  BovaPro 110  effectively  to  reduce  the  spread  of  mastitis  causing  organisms. 

    Recommended  for  pre  and  post  milking  applications.

  • INSTRUCTIONS FOR USE

    DIRECTIONS:

    General Use

    Ready  to  use.  Do  not  dilute.  Do  not  mix  product  with  water,  any  other  teat  dips,  or other product.

    Use  a  teat  dip  cup  to  apply.  Clean  dip  cup  just  prior  to  use.

    If  cow’s teats  are  sore  or chapped,  consult  a  veterinarian  before  starting  or  continuing  to  use  teat  dip.

    If  transferred  from  this  container  to  any  other,  make  sure  that  the  other  container  is  thoroughly  pre-cleaned  and  bears the  proper container labeling  for this  product. 

    If  product  in  dip  cup  becomes  visibly  dirty,  discard  contents  and  replenish  with  undiluted  product. 

    Do  not  reuse  or  return  any  unused  product  to  the  original  container.

    This  product  can  also  be  foamed  or  sprayed  using  recommended  equipment.

    Pre Dipping  Use

    Perform  forestripping  and  inspect  teats  for  clinical  mastitis.

    Pre-wash  teats thoroughly  just  prior  to  milking  with  appropriate  udder  wash  solution  or  pre-milking  teat  dip.  Teats should  then  be  dried  with  single-service  towels.

    Just  before  each  cow  is  milked,  dip,  foam,  or  spray,  each  teat  full-length  into  the  teat  dip  or foam  cup  containing  product.   Allow  product  to  stand  for  30  seconds.

    Wipe teats  dry  after dipping,  using  single-service  towels  to  avoid  contamination  of  milk.

    Post Dipping  Use

    Immediately  after  each  milking,  use  product.

    Dip  each  teat  full-length  into  the  teat  dip  cup  containing  product.  Allow  to  air  dry.   Do  not  wipe.

    If  outside  temperature  is  below  freezing,  allow  to  air  dry  on  the  teat  before  cow  leaves  the  parlor.

    Extended  Use

    When  a  cow  is  being  dried  off,  the  teats should  be  dipped  in  product,  once  a  day  for  3-4  days  after  the  last  milking.  Dipping  should  be  resumed  at  least  twice  daily  one  week  before  calving.

  • SPL UNCLASSIFIED SECTION

    Manufactured By:

    AgroChem USA, LLC 26 Freedom Way • Saratoga Springs, NY 12866 •  (518)226-4850

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    BOVAPRO 110 
    iodine solution solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:17307-3202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    iodine (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) iodine0.01 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17307-3202-119 kg in 1 CONTAINER
    2NDC:17307-3202-257 kg in 1 DRUM
    3NDC:17307-3202-3208 kg in 1 DRUM
    4NDC:17307-3202-41041 kg in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/13/2021
    Labeler - AgroChem USA, LLC (118336116)
    Registrant - AgroChem USA, LLC (118336116)
    Establishment
    NameAddressID/FEIBusiness Operations
    AgroChem USA, LLC118336116api manufacture, manufacture, analysis, label, pack