Home FDA labels 27070a6d-7f65-4ff8-a733-6c9565653187 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 768502e2-541f-4de8-ac68-3ab47c1f436d
SPL ID 27070a6d-7f65-4ff8-a733-6c9565653187
Version 4
Effective date 2024-02-01
Source export date 2026-11-06
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 08:11:28 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 · 24 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 52796-177-90 openfda.package_ndc ndc product 52796-177 openfda.product_ndc ndc11 package 52796017790 derived:openfda.package_ndc spl id 27070a6d-7f65-4ff8-a733-6c9565653187 id spl set id 768502e2-541f-4de8-ac68-3ab47c1f436d 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.