Floravita Mini
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
- Brand name
- Floravita Mini
- Generic name
- FLORAVITA MINI
- Manufacturer
- Florrax Pharmaceutical
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 682bda57-21e0-47df-9596-78846d4d97c0
- SPL ID
- a5d36ac5-e58d-477b-87f2-59fcb0f849e1
- Version
- 3
- Effective date
- 2026-02-12
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:26:35
| 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.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Floravita Mini | openfda.brand_name | |
| generic name | FLORAVITA MINI | openfda.generic_name | |
| manufacturer name | Florrax Pharmaceutical | openfda.manufacturer_name | |
| ndc | package | 84460-907-30 | openfda.package_ndc |
| ndc | product | 84460-907 | openfda.product_ndc |
| ndc11 | package | 84460090730 | derived:openfda.package_ndc |
| spl id | a5d36ac5-e58d-477b-87f2-59fcb0f849e1 | id | |
| spl set id | 682bda57-21e0-47df-9596-78846d4d97c0 | set_id | |
| unii | R5L488RY0Q | openfda.unii | |
| unii | 935E97BOY8 | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | 81G40H8B0T | openfda.unii | |
| unii | P6YC3EG204 | openfda.unii | |
| unii | 1C6V77QF41 | openfda.unii | |
| unii | X66NSO3N35 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Accidental overdose of iron-containing products is a leading cause of fatal poising in children under 6. KEEP THIS PRODUCT OUT OF REACH OF CHILDREN. In the case of accidental overdose, call a doctor or poison control center immediately.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Allergic sensitization has been reported following both oral and parenteral administration of folic acid. You should call your doctor for medical advice about serious adverse events. To reports adverse side effects or to obtain product information, contact Florrax Pharma at 888-321-2821.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.