CALNATE-DMPK (CALCIUM PHOSPHORUS MAGNESIUM POTASSIUM DEXTROSE) SOLUTION [IBA, INC.]

CALNATE-DMPK (CALCIUM PHOSPHORUS MAGNESIUM POTASSIUM DEXTROSE) SOLUTION [IBA, INC.]
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NDC 29983-2712-3
Set ID 53ce90f7-c054-4d9d-8bb9-18c4c47f8ab0
Category OTC ANIMAL DRUG LABEL
Packager IBA, Inc.
Generic Name
Product Class
Product Number
Application Number
  • INDICATIONS & USAGE

    ORAL SOLUTION

    Calcium-Phosphorus-Magnesium-Potassium-Dextrose Oral Solution

    KEEP OUT OF REACH OF CHILDREN

    FOR ANIMAL USE ONLY

    INDICATIONS

    Calnate-DMPK Oral Solution is a cow refreshening mineral supplement to aid maintenance of normal levels of minerals during stressful times of lactation. It contains a scientifically blended amount of calcium, magnesium, phosphorus and potassium in a dextrose solution.

  • DOSAGE AND ADMINISTRATION

    Administer orally as a drench. The usual dose for adult cattle is 500 mL.

  • STORAGE AND HANDLING

    Store at controlled room temperature between 15° and 30°C (59°-86°F)

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • WARNINGS

    Protect for extremes of heat, light and freezing.

  • COMPONENTS

    COMPOSITION:

    Each 500 mL of aqueous solution contains:

    Calcium ............................... 10.0 g

       (as calcium borogluconate)

    Phosphorus .......................... 6.0 g

       (as sodium hypophosphite·H2O)

    Magnesium ........................... 2.8 g

       (as magnesium chloride·6H2O)

    Potassium ............................ 0.5 g

       (as potassium chloride)

    Dextrose·H2O ..................... 75.0 g

    INGREDIENTS:  Dextrose Monohydrate, Glucono Delta Lactone, Boric Acid, Calcium Carbonate, Magnesium Chloride 6·H2O, Potassium Chloride, Propylene Glycol, Sodium Hypophosphite H2O, Ethyl paraben, Methyl paraben, Propyl paraben.

  • PRINCIPAL DISPLAY PANEL

    IBA CMPK

  • INGREDIENTS AND APPEARANCE
    CALNATE-DMPK 
    calcium phosphorus magnesium potassium dextrose solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:29983-2712
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION9 g  in 500 mL
    SODIUM HYPOPHOSPHITE MONOHYDRATE (UNII: 4VN69WUP7N) (HYPOPHOSPHITE ION - UNII:238U65NZ04) PHOSPHATE ION5.4 g  in 500 mL
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CATION2.5 g  in 500 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION0.45 g  in 500 mL
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE75 g  in 500 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29983-2712-3500 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/18/2000
    Labeler - IBA, Inc. (019494160)

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