- 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, phosphorous and potassium deficencies in cattle.
Close - CONTRAINDICATIONS
DO NOT administer this product to animals showing signs of cardiac distress. Monitor animal's condition closely.
Close - 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.
Close - DOSAGE & ADMINISTRATION
Warm solution to body temperature. The usual intravenous dose in cattle is 500 mL per 800 to 1,000 pounds of body weight.
Close - STORAGE
- EACH 500 ML 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...............410 mEq/L
Sodium.......................410 mEq/L
Anions
Borogluconate.........1,341 mEq/L
Chloride.......................410 mEq/L
Hypophosphite..........161 mEq/LOsmolarity (calc.) 11,597 mOsmol/L
Close - CAUTION
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
This product contains no preservatives. Use entire contents when first opened. Discard any unused solution.
Close - C-M-P-K Injection Unit Label
- INGREDIENTS AND APPEARANCE
C-M-P-K
calcium-magnesium -phosphorous-potassium-dextrose injection, solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:60270-121 Route of Administration PARENTERAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 75.0 g in 500 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 8.0 g in 500 mL SODIUM HYPOPHOSPHITE MONOHYDRATE (UNII: 4VN69WUP7N) (HYPOPHOSPHITE ION - UNII:238U65NZ04) PHOSPHATE ION 2.5 g in 500 mL CALCIUM GLUCONATE (UNII: SQE6VB453K) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM GLUCONATE 10.8 g in 500 mL MAGNESIUM GLUCONATE (UNII: T42NAD2KHC) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM GLUCONATE 1.6 g in 500 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60270-121-17 500 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/15/2011 Labeler - VetTek (056387798) Registrant - VetTek (056387798)