Label: BLUEMAX PREMIUM EU- chlorine dioxide liquid

  • NDC Code(s): 48106-1195-1, 48106-1195-2, 48106-1195-3, 48106-1195-4, view more
    48106-1195-5, 48106-1195-6
  • Packager: BouMatic, 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 January 1, 2013

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

  • PRINCIPAL DISPLAY PANEL

    Blank Label

  • INDICATIONS & USAGE

    CHLORINE DIOXIDE SOLUTION
    READY-TO-USE

    INSTRUCTIONS FOR USE :
    NOT FOR HUMAN USE.
    FOR EXTERNAL AND PROFESSIONAL USE ONLY.

    Before milking, treat the entire teat with this product, let act a
    few seconds and wipe teats dry using single-use towels to
    avoid any contamination of milk.

    After milking, treat the entire teat with this product. Allow to
    air dry.

    Note: Replace the visibly dirty solution with fresh solution.
    Do not return unused product to original container.

    EMOLLIENTS 15%
    ACTIVE SUBSTANCE (0,9 % Chlorine Dioxide)

    Caution: the equipment must be adapted to contact with
    chlorine dioxide

  • PEDIATRIC USE

    FIRST AID:

    If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes.
    Remove contact lenses, if present after the first 5 minutes, then continue rinsing. Contact a
    physician immediately.
    If swallowed: Have person sip a glass of water if able to swallow. Do not give anything to
    an unconscious person. Do not induce vomiting. Contact a physician immediately.
    If breathing difficulty occurs: Move person to fresh air. Contact a physician
    immediately.
    If on skin: If irritation develops and persists, contact a physician.
    Have the product container or label with you when going for treatment, calling a physician,
    the emergency number listed on this label or MSDS, or a poison control center.
    PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals. Only use
    in one ventilated areas.

    STORAGE: Store in a closed container away from sources of heat. If product becomes
    frozen, thaw and mix well before use.

    Remember these industry guidelines:
    Always use caution when introducing your cows to a new product.
    Replace applicator. When introducing a new solution to a dairy herd, always replace
    applicator to prevent the new solution from mixing with the old applicator. If pumps are
    used, lines should be flushed with hot water to clean out any residues of the old solution.

    Aggressively remove keratin and exfoliated skin from teats
    A temporary exfoliation of dead teat skin is common after new solution are introduced. Be
    sure to aggressively clean teats to remove exfoliated skin and clean teat ends to insure that
    the dead skin is removed.

    Monitor cows for changes in skin condition
    Many solutions are designed with emollients and other skin conditioning ingredients to
    maintain healthy teat skin and fight germs. Rare teat skin reactions due to allergic or
    environmental conditions may occur. Closely monitor teat skin whenever a new solution is
    introduced. If unusual skin conditions are found, monitor closely and, if persistent, replace
    solution with one containing a different germicide and/or emollient formula

  • INGREDIENTS AND APPEARANCE
    BLUEMAX PREMIUM EU 
    chlorine dioxide liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-1195
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE32 g  in 10 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48106-1195-13.8 L in 1 DRUM
    2NDC:48106-1195-218.9 L in 1 DRUM
    3NDC:48106-1195-356.8 L in 1 DRUM
    4NDC:48106-1195-4114 L in 1 DRUM
    5NDC:48106-1195-5208 L in 1 DRUM
    6NDC:48106-1195-61040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2013
    Labeler - BouMatic, LLC (124727400)
    Registrant - BouMatic, LLC (124727400)
    Establishment
    NameAddressID/FEIBusiness Operations
    BouMatic, LLC124727400manufacture, api manufacture