FDA.reportPublic FDA data

NDC 13985-805 - CMPK

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
13985-805
Package NDCs from labels
13985-805-50
Manufacturer
MWI (VetOne)
Effective date
2026-03-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CMPK - MWI (VetOne)MWI (VetOne)2026-03-20PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-805-50CMPK500 mL in 1 BOTTLE, PLASTICINJECTION, SOLUTION5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-805CMPK INJECTION, SOLUTION [MWI (VETONE)]31 package rows20151217_f2b27f49-9707-480c-90d8-430a09ef6c03.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Calcium Gluconate MonohydrateACTIVE INGREDIENTCZN0MI5R31CMPK INJECTION, SOLUTION [MWI (VETONE)]2
Dextrose MonohydrateACTIVE INGREDIENTLX22YL083GCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Magnesium GluconateACTIVE INGREDIENTT42NAD2KHCCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Potassium ChlorideACTIVE INGREDIENT660YQ98I10CMPK INJECTION, SOLUTION [MWI (VETONE)]2
Sodium Hypophosphite MonohydrateACTIVE INGREDIENT4VN69WUP7NCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Calcium CationACTIVE MOIETY2M83C4R6ZBCMPK INJECTION, SOLUTION [MWI (VETONE)]2
DextroseACTIVE MOIETYIY9XDZ35W2CMPK INJECTION, SOLUTION [MWI (VETONE)]2
Magnesium cationACTIVE MOIETYT6V3LHY838CMPK INJECTION, SOLUTION [MWI (VETONE)]2
PhosphorusACTIVE MOIETY27YLU75U4WCMPK INJECTION, SOLUTION [MWI (VETONE)]2
Potassium cationACTIVE MOIETY295O53K152CMPK 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 13 of 31 · 616 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Schuessler Tissue Salts Comb D Skin DisordersKALI MURIATICUM,KALI SULPHURICUM,CALCAREA SULPHURICA,SILICEAMartin & Pleasance Pty Ltd03153d92-dc68-4b84-a8c9-634b1ffd7da12025-08-13WarningsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEHenry Schein, Inc.bf8e8ac7-e6a8-4571-a0ea-7bcab89290f62025-08-12Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEAvKARE3bdfced1-6e62-9e92-e063-6294a90a28aa2025-08-08Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium Chloride Extended-ReleasePOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC3be29fcc-765e-8653-e063-6394a90a59d52025-08-08Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDESlate Run Pharmaceuticals, LLC94ae03cc-b620-0dbb-e053-2a95a90a922c2025-08-07Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDESlate Run Pharmaceuticals, LLC0cc57ece-f15a-4160-a5ea-8d6fa9f9e7542025-08-07Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEPD-Rx Pharmaceuticals, Inc.47a87fb6-5e61-41c9-b759-10f7c74a67ce2025-08-05Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEAmerican Health Packaging7956883f-0d31-4081-bbea-d9ea320a193b2025-08-04Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium Chloride for Oral SolutionPOTASSIUM CHLORIDE FOR ORAL SOLUTIONMarlex Pharmaceuticals Inc3e78028d-21a0-ba0f-e063-6294a90aac492025-08-01Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium Chloride for Oral SolutionPOTASSIUM CHLORIDE FOR ORAL SOLUTIONMarlex Pharmaceuticals, Inc.3e8a6f61-44eb-4b5a-e063-6294a90a4b1b2025-08-01Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDE EXTENDED RELEASEPOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC3b403d60-4246-d765-e063-6394a90a12e82025-07-31Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEA-S Medication Solutions162a8ab5-76cf-48fa-8487-7780ed65647e2025-07-31Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEA-S Medication Solutions14db14ba-fd0d-4b2a-9f1c-a62b3b82306f2025-07-31Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
DextroseDEXTROSE MONOHYDRATEBaxter Healthcare Companybfc4224a-2fc9-4137-b4c6-9d2d6d9484132025-07-30Warnings, Adverse reactionsExact identifier
unii: LX22YL083G
Cell SaltsCALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEANewton Laboratories, Inc.985a3341-0fe0-1dd6-e053-2a95a90ad2c52025-07-25WarningsExact identifier
unii: 660YQ98I10
Cell SaltsCALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEANewton Laboratories, Inc.7a1b4e96-c96f-6424-e053-2991aa0aef302025-07-24WarningsExact identifier
unii: 660YQ98I10
Cell SaltsCALC. FLUOR., CALC. PHOS., CALC.SULPH., FERRUM PHOSPHORICUM, KALI MUR., KALI PHOS., KALI SULPH., MAG. PHOS., NAT. MUR., NAT. PHOS., NAT.SULPHURICUM, SILICEANewton Laboratories, Inc.7a1a9ef9-9a54-5f94-e053-2a91aa0ab4772025-07-24WarningsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEAvKARE8baf3f25-c78b-6c08-e053-2995a90a667e2025-07-23Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEAvKARE8bb030b7-104a-373b-e053-2995a90ab5802025-07-23Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEGuardian Drug Company296eda62-ea8e-7a0c-e063-6294a90a92742025-07-22Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

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