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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
52796-170-50	ML - Milliliter	52796-170	02efcbac-9796-473b-8477-1728b4f6e1a7	1	2018-04-19

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 98 of 98 · 1,944 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SF 5000 Plus	1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM	Cypress Pharmaceutical, Inc.	fa625ece-d873-491a-8d45-2833b64e5425	2016-07-01	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Ionite H	SODIUM FLUORIDE, POTASSIUM NITRATE	Dharma Research, Inc.	54c1a27c-5936-4ee2-a419-3891d3df9745	2015-08-02	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Ionite H	SODIUM FLUORIDE, POTASSIUM NITRATE	Dharma Research, Inc.	642fec99-c5c5-4ef2-986e-5b5f7cf460de	2015-08-02	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7

Reported adverse events (FAERS/openFDA)#

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