NDC 48106-2004 - Udderdine 102 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
48106-2004
Package NDCs from labels
48106-2004-1, 48106-2004-2, 48106-2004-3, 48106-2004-4
Manufacturer
BouMatic, LLC
Effective date
2024-06-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Udderdine 102 NPE Free - BouMatic, LLCBouMatic, LLC2024-06-14OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48106-2004-1Udderdine 102 NPE Free19 L in 1 DRUMLIQUID192
48106-2004-2Udderdine 102 NPE Free56.8 L in 1 DRUMLIQUID56.82
48106-2004-3Udderdine 102 NPE Free208 L in 1 DRUMLIQUID2082
48106-2004-4Udderdine 102 NPE Free1041 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID10412

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48106-2004UDDERDINE 102 NPE FREE (IODINE TEAT DIP) LIQUID [BOUMATIC, LLC]24 package rows20240616_c84d5775-496c-48ff-b3e3-cabe3f3c9bc9.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.