C-M-P-K description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

C-M-P-K

VetTek
VetTek

C-M-P-K Injection


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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.

C-M-P-K CONTRAINDICATIONS

DO NOT administer this product to animals showing signs of cardiac distress. Monitor animal's condition closely.

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.

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.

STORAGE

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

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/L

Osmolarity (calc.) 11,597 mOsmol/L

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.

C-M-P-K Injection Unit Label

C-M-P-K

C-M-P-K

Calcium-Magnesium -Phosphorous-Potassium-Dextrose INJECTION, SOLUTION

Product Information

Product Type Prescription animal drug label Item Code (Source) NDC:60270-121
Route of Administration PARENTERAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Dextrose monohydrate ANHYDROUS DEXTROSE 75.0 g
potassium chloride 8.0 g
SODIUM HYPOPHOSPHITE MONOHYDRATE Phosphorus 2.5 g
Calcium Gluconate 10.8 g
MAGNESIUM GLUCONATE Magnesium cation 1.6 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60270-121-17 500 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-06-15


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.