Milk Fever CP

Manufacturer
Aspen Veterinary
Effective date
2025-09-09
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:45:00

Label at a glance#

ProductMilk Fever CP
Active ingredientCalcium Borogluconate, Dextrose Monohydrate, Magnesium Gluconate, Phosphorus
Label structure13 sections

Storage and handling

Store between 15 degrees C-30 degrees C (59degrees F-86 degrees F).

Label contents#

Full prescribing information#

CAUTION:

PRECAUTIONS SECTION

Federal law restricts this drug to use
by or on the order of a licensed veterinarian.

GENERAL PRECAUTIONS SECTION

For Animal Use Only
Keep Out of Reach of Children

INFORMATION FOR OWNERS/CAREGIVERS SECTION

NET CONTENTS:
500 mL (16.91 fl oz)

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Parenteral Solution

INDICATIONS:

INDICATIONS & USAGE SECTION

For intravenous use in milk fever, and in calcium,
phosphorus, magnesium and glucose deficiency
in animals.

NOTE:

INDICATIONS & USAGE SECTION

Intravenous administration is always preferable.
If used subcutaneously, always distribute dose
in several places and massage to facilitate
absorption.

DOSAGE:

DOSAGE & ADMINISTRATION SECTION

Cattle, 500 mL. For milk fever prophylaxis, give
200-500 mL at time of calving. Horses, 250-500
mL; Sheep 50-125 mL. Repeat in 2 to 6 hours if
needed. This product contains no preservative.
Unused portion remaining in bottle must be
discarded.

CAUTION:

GENERAL PRECAUTIONS SECTION

Large doses administered intravenously may have
toxic action on heart if the blood level of calcium
is raised excessively. Doses should be carefully
regulated according to severity of hypocalcemia
and injected slowly so that administration may be
stopped if toxic action becomes evident.

CONTAINS:

DOSAGE FORMS & STRENGTHS SECTION

Calcium borogluconate, dextrose, magnesium
borogluconate, calcium hypophosphite and base.

Total calcium chemically equivalent to calcium
borogluconate...................................26.0% w/v
Dextrose . H2O..................................15.0% w/v
Magnesium borogluconate..................6.0% w/v
Total phosphorus in amounts chemically
equivalent to elemental phosphorus.....0.5% w/v

STORAGE AND HANDLING SECTION

Store between 15 degrees C-30 degrees C (59degrees F-86 degrees F).

GENERAL PRECAUTIONS SECTION

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Distributed by:
Aspen Veterinary ResourcesR, Ltd.
Liberty, MO 64068 USA
www.aspenveterinaryresources.com

Manufactured by:
Nova-Tech, Inc.
Grand Island, NE 68801 USA      18-811        RMS# 92-565

Lot No.             Exp. Date

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

container labelcontainer label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427
MAGNESIUM CATION Pharmacologic Class Indexing4Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46066-811-50Milk Fever CP500 mL in 1 BOTTLE, PLASTICINJECTION, SOLUTION5003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Calcium BorogluconateACTIVE INGREDIENT6915G2PQI01
Dextrose MonohydrateACTIVE INGREDIENTLX22YL083G1
Magnesium GluconateACTIVE INGREDIENTT42NAD2KHC1
PhosphorusACTIVE INGREDIENT27YLU75U4W1
Anhydrous DextroseACTIVE MOIETY5SL0G7R0OK1
Calcium CationACTIVE MOIETY2M83C4R6ZB1
Magnesium CationACTIVE MOIETYT6V3LHY8381
PhosphorusACTIVE MOIETY27YLU75U4W1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46066-81146066-811-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.