Label: C-M-P-K injection, solution

  • Category: PRESCRIPTION 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 November 1, 2019

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

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS:

    For use as an aid in the treatment of hypocalcemia (parturient paresis, milk fever), hypomagnesemia (grass tetany), and other conditions associated with calcium, magnesium, phosphorus and potassium deficiencies in cattle.

  • CONTRAINDICATIONS:

    Do not administer this product to animals showing signs of cardiac distress.

  • PRECAUTIONS:

    Administration should be made slowly and with care to avoid adverse effects such as heart block or shock. Perivascular or subcutaneous deposition of hypertonic solutions may result in severe inflammation at the injection site.

  • CAUTION:

    This product contains no preservatives. Use entire contents when first opened. Discard any unused solution.

  • DOSAGE AND ADMINISTRATION:

    Warm solution to body temperature. The usual intravenous dose in cattle is 500 mL per 800 to 1,000 pounds of body weight.

  • STORAGE AND HANDLING

    Store between 15°C and 30°C (59°F and 86°F)

  • VETERINARY INDICATIONS

    FOR ANIMAL USE ONLY

  • CAUTION:

    Federal law restricts this drug to use by or on the order of a licensed veterinarian.

  • COMPOSITION:

    Each 500 mL of sterile aqueous solution contains:
    Calcium............................10.8 g
    (as calcium borogluconate, equivalent to calcium gluconate 23.2%)
    Potassium..........................8.0 g
    (as potassium chloride)
    Phosphorus.......................2.5 g
    (as sodium hypophosphite • H2O)
    Magnesium.......................1.6 g
    (as magnesium borogluconate)
    Dextrose •H2O................75.0 g
    Milliequivalents per liter

    Cations
    Calcium......................1,080 mEq/L
    Potassium.....................410 mEq/L
    Magnesium...................261 mEq/L
    Sodium.........................161 mEq/L

    Anions
    Borogluconate....................1,341 mEq/L
    Chloride................................410 mEq/L
    Hypophosphite......................161 mEq/L

  • INFORMATION FOR OWNERS/CAREGIVERS

    Manufactured for
    VetTek
    Blue Springs, MO 64014

    REV 06-19

  • PRINCIPAL DISPLAY PANEL

    NDC 60270-128-17

    C-M-P-K Injection

    CALCIUM-MAGNESIUM-PHOSPHORUS-POTASSIUM-DEXTROSE SOLUTION

    Dura-Ster TS

    TERMINALLY STERILIZED

    Net Contents: 500 mL (16.9 fl. oz.)

    Label

  • INGREDIENTS AND APPEARANCE
    C-M-P-K 
    c-m-p-k injection, solution
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:60270-128
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM GLUCONATE MONOHYDRATE (UNII: CZN0MI5R31) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM GLUCONATE MONOHYDRATE10.8 g  in 500 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION8.0 g  in 500 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS2.5 g  in 500 mL
    MAGNESIUM GLUCONATE (UNII: T42NAD2KHC) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM GLUCONATE1.6 g  in 500 mL
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE75.0 g  in 500 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60270-128-17500 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/01/2019
    Labeler - VetTek (056387798)
    Registrant - VetTek (056387798)