Home NDC 52796-170 NDC 52796-170 - Floriva Plus 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 52796-170
Package NDCs from labels 52796-170-50
Manufacturer BonGeo Pharmaceuticals, Inc.
Effective date 2018-04-04
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Floriva Plus Liquid Drops ™ BonGeo Pharmaceuticals, Inc. 2018-04-04 DIETARY SUPPLEMENT
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52796-170-50 Floriva Plus 50 mL in 1 CONTAINER SOLUTION/ DROPS 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52796-170 FLORIVA PLUS (VITAMIN A PALMITATE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL SUCCINATE, D-, THIAMINE HYDROCHLORIDE, RIBOFLAVIN 5-PHOSPHATE SODIUM, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, LEVOMEFOLATE GLUCOSAMINE, CYANOCOBALAMIN, AND SODIUM FLUORIDE) SOLUTION/ DROPS [BONGEO PHARMACEUTICALS, INC.] 2 1 package rows 20180405_790120de-fd34-4be8-bc2a-8e03e5dc987b.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 35 of 99 · 1,980 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.