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MAGNA

Pegasus Laboratories, Inc.
Pegasus Laboratories, Inc.

MAGNA GEL


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DESCRIPTION:

A Nutritional Supplement Supplying Additional Magnesium and Calcium For Beef and Dairy Cattle

GUARANTEED ANALYSIS:

Unless otherwise stated, values listed are minimums.

Magnesium...............................2.0%

Calcium (Max)...........................0.6%

Calcium ...................................0.1%

INGREDIENTS:

Magnesium Chloride, Hydroxyethyl Cellulose, Propylene Glycol, Glycerin, Calcium Chloride, Methyl Paraben (preservative), Propyl Paraben (preservative), Potassium Sorbate (preservative), Mint Green Color.

STORAGE:

Store in a cool dry place.

WARNINGS:

This product is intended for intermittent use or supplemental feeding only.

Do not feed to animals with mouth or throat sores.

Keep out of reach of children.

For livestock use only.

Use only as directed.

Not for human use.

For veterinary use only.

USE:

MAGNA GEL™ is intended as an oral supplement of Magnesium and Calcium for Beef and Dairy Cattle.

DIRECTIONS FOR USE:

Dairy and Beef Cattle:

Give two tubes daily, as condition requires.

Hold animal's head in a slightly elevated position. Insert the nozzle of syringe through the interdental space and quickly squeeze product to the back of the animal's mouth.  Hold mouth closed until product is swallowed. Do not use a rope or restraint that could choke the animal.

SAFETY:

Use extreme caution to prevent injury to mouth or throat tissue; do not allow the animal to chew on the tip of the tube, which can result in mouth lacerations.

CAUTION:

Contact with the skin, wounds or prolonged contact with the skin can cause irritation, flush with warm water if exposed.

PRINCIPAL DISPLAY PANEL:

PRN PHARMACAL MAGNA GEL™

MANUFACTURED FOR

PRN PHAMACAL

Employee-Owned

PENSACOLA, FL 32514

CONTENTS: 10 FL OZ (300mL)

MAGNA

MAGNA

Magnesium, Calcium GEL

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:49427-013
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM CHLORIDE ANHYDROUS CALCIUM CATION 1 mg
MAGNESIUM CHLORIDE 20 mg

Inactive Ingredients

Ingredient Name Strength
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
water
POTASSIUM SORBATE
GLYCERIN
METHYLPARABEN
PROPYLPARABEN
propylene glycol

Product Characteristics

Color
green (light green)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49427-013-33 300 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1990-04-01


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