MILK FEVER- milk fever calcium liquid

Milk Fever by

Drug Labeling and Warnings

Milk Fever by is a Animal medication manufactured, distributed, or labeled by Radix Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CONTENTS (per 360ml):

• Calcium Chloride (as anhydrous).........10.0g
• Phosphates........................................6.2g
• Potassium..........................................4.5g
• Magnesium (as Chloride 6 H2O USP).....3.0g
• Total Calcium Ions = 45 gms

Inactives:

• HEC, Molasses, Purified Water, Sodium Benzoate

MEq VALUES:

• Calcium..............2252 MEq
• Magnesium...........246 MEq
• Phosphate...........66.0 MEq
• Potassium............120 MEq

INDICATIONS:

• A supplemental source of calcium, phosphorus, magnesium, and potassium as an oral follow-up to milk fever therapy in cattle.

Storage:

• Store at controlled room temperature between 59oF to 86oF (15oC -30oC).

Warning:

• Shake well before use
• Administer with care to avoid aspiration.
• FOR ANIMAL USE ONLY

Dosage and administration:

• Administer orally at the rate of 1 fluid ounce per 100 pounds animal body weight or as directed by your veterinarian.
• No milk withdrawal
• No slaughter withdrawal

KEEP OUT OF REACH OF CHILDREN

• Keep away from children.

Current MFDR Gallon Label

Item Image

INGREDIENTS AND APPEARANCE

MILK FEVER 
milk fever calcium liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 50480-130
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CHLORIDE	125 g  in 360 mL
SODIUM HYPOPHOSPHITE (UNII: 8TU1537O43) (HYPOPHOSPHITE ION - UNII:238U65NZ04)	SODIUM HYPOPHOSPHITE MONOHYDRATE	6.2 g  in 360 mL
MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM CHLORIDE	3.0 g  in 360 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	4.5 g  in 360 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50480-130-40	4 in 1 CARTON
1		3785 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/27/2013

Labeler - Radix Laboratories, Inc. (108500091)