NDC 29983-0080 - ICON 5000 II NPE FREE

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
29983-0080
Package NDCs from labels
29983-0080-6, 29983-0080-4, 29983-0080-8, 29983-0080-9
Manufacturer
IBA
Effective date
2013-12-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ICON 5000 II NPE FREE - IBAIBA2013-12-17OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
29983-0080-4ICON 5000 II NPE FREE18.9 L in 1 PACKAGESOLUTION, CONCENTRATE18.92
29983-0080-6ICON 5000 II NPE FREE56.7 L in 1 DRUMSOLUTION, CONCENTRATE56.72
29983-0080-8ICON 5000 II NPE FREE207.9 L in 1 DRUMSOLUTION, CONCENTRATE207.92
29983-0080-9ICON 5000 II NPE FREE1039.5 L in 1 DRUMSOLUTION, CONCENTRATE1039.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
29983-0080ICON 5000 II NPE FREE SOLUTION, CONCENTRATE [IBA]24 package rows20250101_947dfd83-8a4b-4e9e-bdd0-b830fba4045d.zip

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 12 of 12 · 222 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bio IodineIODIUMBioActive Nutritional, Inc.69be0ca4-99b7-4de0-b4f2-5723b1f1a7da2016-08-11WarningsExact identifier
unii: 9679TC07X4
ThyrotoxCHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEABioActive Nutritional, Inc.e229a260-13f3-4136-b325-9a8954f8a3272016-08-10WarningsExact identifier
unii: 9679TC07X4

Reported adverse events (FAERS/openFDA)#

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