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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
- STORAGE AND HANDLING
- WARNINGS
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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
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INGREDIENTS AND APPEARANCE
CALNATE-DMPK
calcium phosphorus magnesium potassium dextrose solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:29983-2712 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 9 g in 500 mL SODIUM HYPOPHOSPHITE MONOHYDRATE (UNII: 4VN69WUP7N) (HYPOPHOSPHITE ION - UNII:238U65NZ04) PHOSPHATE ION 5.4 g in 500 mL MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CATION 2.5 g in 500 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 0.45 g in 500 mL DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 75 g in 500 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29983-2712-3 500 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/18/2000 Labeler - IBA, Inc. (019494160)