NDC 17307-3123 - BovaPro 102 Teat Dip

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
17307-3123
Package NDCs from labels
17307-3123-1, 17307-3123-2, 17307-3123-3, 17307-3123-4
Manufacturer
AgroChem Inc
Effective date
2018-01-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
BovaPro 102 Teat Dip - AgroChem IncAgroChem Inc2018-01-26OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17307-3123-1BovaPro 102 Teat Dip19 kg in 1 CONTAINERSOLUTION192
17307-3123-2BovaPro 102 Teat Dip57 kg in 1 DRUMSOLUTION572
17307-3123-3BovaPro 102 Teat Dip208 kg in 1 DRUMSOLUTION2082
17307-3123-4BovaPro 102 Teat Dip1040 kg in 1 CONTAINERSOLUTION10402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17307-3123BOVAPRO 102 TEAT DIP (IODINE) SOLUTION [AGROCHEM INC]24 package rows20180126_d7ea369d-3aa2-4f3a-aa10-572bedcd7392.zip

DailyMed Socrata Ingredients#

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 38 of 38 · 742 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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