Label: BOVA PRO 105- iodine spray

  • NDC Code(s): 17307-1051-1, 17307-1051-2, 17307-1051-3, 17307-1051-4
  • Packager: AgroChem Inc
  • 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 August 20, 2013

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

  • PRECAUTIONS

    CONCENTRATE/MUST BE DILUTED FOR USE!  NOTE:  PRODUCT MAY SEPARATE IN STORAGE/

    MIX THOROUGHLY BEFORE USING. (1:4 Mix by Volume)

    AVOID FREEZING -

    PRODUCT WILL BECOME

    THICKER WITH COLD 

  • DESCRIPTION

    BovaPro Teat Spray is an aid in the

    prevention of organisms which may

    cause mastitis. 

  • ACTIVE INGREDIENT

    INGREDIENTS:  WHEN MIXED FOR USE

    Active Ingredient - Iodine 1.0%

    Emollients - 5.0%

  • WARNINGS

    WARNING:  keep away from children.  If

    accidentally swallowed or taken

    internally, contact physician

    immediately.

    IMPORTANT:  THIS IS A CONCENTRATE

    AND MUST BE DILUTED WITH WATER

    PRIOR TO USE.  Mix one part concentrate to

    four parts of clean soft water.  (mix by

    volume) 

  • INSTRUCTIONS FOR USE

    DIRECTIONS FOR USE:  Immediately after each cow

    is milked, spray, dip or foam teats with a (1:4) diluted

    solution of BovaPro 105 concentrated Teat Spray.

    The solution should be applied to the teat up to the

    base of the udder.  At the end of lactation, the teats

    should be sprayed, dipped or foamed with BovaPro

    Teat Spray for four days after last milking.  If the

    solution is visibly dirty or contains sediment, use fresh

    solution.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    BOVA PRO 105  
    iodine spray
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:17307-1051
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE.01 kg  in 1 kg
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) .025 kg  in 1 kg
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .025 kg  in 1 kg
    WATER (UNII: 059QF0KO0R) .025 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17307-1051-119 kg in 1 CONTAINER
    2NDC:17307-1051-257 kg in 1 DRUM
    3NDC:17307-1051-3208 kg in 1 DRUM
    4NDC:17307-1051-41040 kg in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/01/2013
    Labeler - AgroChem Inc (805427700)
    Establishment
    NameAddressID/FEIBusiness Operations
    AgroChem Inc805427700manufacture, api manufacture