Floriva

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Floriva
Generic name: VITAMIN A ACETATE, .BETA.-CAROTENE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, AND SODIUM FLUORIDE
Manufacturer: BonGeo Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 3d5fbe3a-a95b-4688-a96e-b34e6e1e868a
SPL ID: fc2600e1-f961-4c00-9810-5612e8dfaaff
Version: 4
Effective date: 2024-02-01
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:14:27

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Floriva	openfda.brand_name
generic name		VITAMIN A ACETATE, .BETA.-CAROTENE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, LEVOMEFOLATE GLUCOSAMINE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, ZINC GLUCONATE, CUPRIC OXIDE, AND SODIUM FLUORIDE	openfda.generic_name
manufacturer name		BonGeo Pharmaceuticals, Inc.	openfda.manufacturer_name
ndc	package	52796-173-12	openfda.package_ndc
ndc	package	52796-173-90	openfda.package_ndc
ndc	product	52796-173	openfda.product_ndc
ndc11	package	52796017390	derived:openfda.package_ndc
ndc11	package	52796017312	derived:openfda.package_ndc
spl id		fc2600e1-f961-4c00-9810-5612e8dfaaff	id
spl set id		3d5fbe3a-a95b-4688-a96e-b34e6e1e868a	set_id
unii		01YAE03M7J	openfda.unii
unii		25X51I8RD4	openfda.unii
unii		3LE3D9D6OY	openfda.unii
unii		TLM2976OFR	openfda.unii
unii		8ZYQ1474W7	openfda.unii
unii		935E97BOY8	openfda.unii
unii		PQ6CK8PD0R	openfda.unii
unii		V1XJQ704R4	openfda.unii
unii		Q65PL71Q1A	openfda.unii
unii		6SO6U10H04	openfda.unii
unii		P6YC3EG204	openfda.unii
unii		U6WSN5SQ1Z	openfda.unii
unii		KV2JZ1BI6Z	openfda.unii
unii		1C6V77QF41	openfda.unii
unii		X66NSO3N35	openfda.unii
unii		H4N855PNZ1	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNING KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. IF OVERDOSAGE IS SUSPECTED, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY 1-800-222-1222. TABLET SHOULD BE CHEWED. THIS TABLET, AS WITH ALL TABLETS, IS NOT RECOMMENDED FOR CHILDREN UNDER AGE OF 4 DUE TO RISK OF CHOKING.

Reported adverse events (FAERS/openFDA)#

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