NDC 13985-811 - CalPlus

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 13985-811
Package NDCs from labels: 13985-811-50
Manufacturer: MWI (VetOne)
Effective date: 2025-09-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CalPlus - MWI (VetOne)	MWI (VetOne)	2025-09-09	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
13985-811-50	CalPlus	500 mL in 1 BOTTLE, PLASTIC	INJECTION, SOLUTION	500		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
13985-811	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2	1 package rows	20140609_baf30e03-36ed-43b0-9db7-34d020934733.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Calcium Borogluconate	ACTIVE INGREDIENT	6915G2PQI0	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
DEXTROSE MONOHYDRATE	ACTIVE INGREDIENT	LX22YL083G	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
Magnesium Gluconate	ACTIVE INGREDIENT	T42NAD2KHC	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
Phosphorus	ACTIVE INGREDIENT	27YLU75U4W	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
ANHYDROUS DEXTROSE	ACTIVE MOIETY	5SL0G7R0OK	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
Calcium Cation	ACTIVE MOIETY	2M83C4R6ZB	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
Magnesium cation	ACTIVE MOIETY	T6V3LHY838	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2
Phosphorus	ACTIVE MOIETY	27YLU75U4W	CALPLUS INJECTION, SOLUTION [MWI (VETONE)]	2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 42 of 42 · 824 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Inflammation II	ASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), SARSAPARILLA (SMILAX REGELII), TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, THYROIDINUM (SUIS), AURUM METALLICUM, CARBO ANIMALIS, CAUSTICUM, GELSEMIUM SEMPERVIRENS, NATRUM SULPHURICUM, PHOSPHORUS, SULPHUR, THUJA OCCIDENTALIS	BioActive Nutritional, Inc.	4c36e714-f564-41d3-a6b8-60e633defaff	2016-10-04	Warnings	Exact identifier unii: 27YLU75U4W
Thyrotox	CHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA	BioActive Nutritional, Inc.	e229a260-13f3-4136-b325-9a8954f8a327	2016-08-10	Warnings	Exact identifier unii: 27YLU75U4W
Cerebroforce	CAPSICUM ANNUUM, GINKGO BILOBA, GELSEMIUM SEMPERVIRENS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, ARSENICUM ALBUM	BioActive Nutritional, Inc	f998ed3f-56a5-4497-be5b-9a819fe8be69	2016-07-13	Warnings	Exact identifier unii: 27YLU75U4W
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: LX22YL083G

Reported adverse events (FAERS/openFDA)#

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