NDC 23594-700 - Tri-Vi-Flor

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
23594-700
Package NDCs from labels
23594-700-50
Manufacturer
Aytu Therapeutics LLC
Effective date
2023-09-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tri-Vi-Flor - Aytu Therapeutics LLCAytu Therapeutics LLC2023-09-29DIETARY SUPPLEMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23594-700-50Tri-Vi-Flor1 in 1 PACKAGESUSPENSION/ DROPS17
23594-700-50Tri-Vi-Flor50 mL in 1 BOTTLESUSPENSION/ DROPS507

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23594-700TRI-VI-FLOR (MULTIVITAMIN AND FLUORIDE SUPPLEMENT) SUSPENSION/ DROPS [AYTU THERAPEUTICS LLC]72 package rows20240123_40130338-ee51-42c9-babb-c4aab442d3f4.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23594-700-50ML - Milliliter23594-700f3d3867e-9923-4e89-9dec-35bc126f5fe512016-10-06

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 51 of 71 · 1,411 matching rows.

Brand, Generic, Manufacturer table
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Reported adverse events (FAERS/openFDA)#

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