CalPlus

Manufacturer
MWI (VetOne)
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#

ProductCalPlus
Active ingredientCalcium Borogluconate, DEXTROSE MONOHYDRATE, Magnesium Gluconate, Phosphorus
Label structure10 sections

Dosage and administration

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.  Intravenous administration is always preferable.  If used subcutaneously, always distribute dose in several places and massage to facilitate absorption.  This product contains no preservative.  Unused portion remaining in bottle must be discarded.

Storage and handling

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

Label contents#

Full prescribing information#

CONTAINS:

DOSAGE FORMS & STRENGTHS SECTION

Calcium borogluconate, dextrose, magnesium
borogluconate, calcium hypo-phosphite.
Total calcium chemically equivalent
to calcium borogluconate .................................... 26.0% w/v
Dextrose H20 .................................................... 15.0% w/v
Magnesium borogluconate .................................... 6.0% w/v
Total phosphorus in amounts chemically
equivalent to elemental phosphorus ....................... 0.5% w/v

INDICATIONS:

INDICATIONS & USAGE SECTION

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

DOSAGE AND ADMINISTRATION:

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.  Intravenous administration is always
preferable.  If used subcutaneously, always distribute dose in
several places and massage to facilitate absorption.  This
product contains no preservative.  Unused portion remaining
in bottle must be discarded.

GENERAL PRECAUTIONS SECTION

Parental Solution

For animal use only.

Keep out of reach of children.

CAUTION:

INDICATIONS & USAGE SECTION

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

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.

STORAGE:

STORAGE AND HANDLING SECTION

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

GENERAL PRECAUTIONS SECTION

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Manufactured by:
Nova-Tech, Inc.
Grand Island, NE 68801

Distributed by: MWI
Boise, ID 83705
(888) 694-8381
www.vetone.net

V1 510122      Net Contents: 500 mL

Rev. 06-11

18-811-50       RMS 92-590

Lot#        Exp.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MWI CalPlus Container LabelMWI CalPlus Container 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
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-811-50CalPlus500 mL in 1 BOTTLE, PLASTICINJECTION, SOLUTION5003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Calcium BorogluconateACTIVE INGREDIENT6915G2PQI02
DEXTROSE MONOHYDRATEACTIVE INGREDIENTLX22YL083G2
Magnesium GluconateACTIVE INGREDIENTT42NAD2KHC2
PhosphorusACTIVE INGREDIENT27YLU75U4W2
ANHYDROUS DEXTROSEACTIVE MOIETY5SL0G7R0OK2
Calcium CationACTIVE MOIETY2M83C4R6ZB2
Magnesium cationACTIVE MOIETYT6V3LHY8382
PhosphorusACTIVE MOIETY27YLU75U4W2

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
13985-81113985-811-50

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 · Source PDF

Reported adverse events (FAERS/openFDA)#

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