adverse reactions
ADVERSE REACTIONS Allergic sensitizations have been reported following oral administration of folic acid. Consult your physician immediately if adverse side effects occur.
Dialyvite
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
- Dialyvite
- Generic name
- ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, FOLIC ACID, COBALAMIN, BIOTIN, PANTOTHENIC ACID
- Manufacturer
- Hillestad Pharmaceuticals USA
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7a5e6dd6-5687-44bb-8964-841961c0e64a
- SPL ID
- c91498fd-0515-46a9-8a22-e423f554bd86
- Version
- 5
- Effective date
- 2026-01-27
- Source export date
- 2026-10-27
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:59:59
| 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 | Dialyvite | openfda.brand_name | |
| generic name | ASCORBIC ACID, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, FOLIC ACID, COBALAMIN, BIOTIN, PANTOTHENIC ACID | openfda.generic_name | |
| manufacturer name | Hillestad Pharmaceuticals USA | openfda.manufacturer_name | |
| ndc | package | 10542-010-02 | openfda.package_ndc |
| ndc | package | 10542-010-10 | openfda.package_ndc |
| ndc | product | 10542-010 | openfda.product_ndc |
| ndc11 | package | 10542001002 | derived:openfda.package_ndc |
| ndc11 | package | 10542001010 | derived:openfda.package_ndc |
| spl id | c91498fd-0515-46a9-8a22-e423f554bd86 | id | |
| spl set id | 7a5e6dd6-5687-44bb-8964-841961c0e64a | set_id | |
| unii | 25X51I8RD4 | openfda.unii | |
| unii | TLM2976OFR | openfda.unii | |
| unii | 935E97BOY8 | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | 568ET80C3D | openfda.unii | |
| unii | 6SO6U10H04 | openfda.unii | |
| unii | 8K0I04919X | openfda.unii | |
| unii | 68Y4CF58BV | openfda.unii | |
| unii | 8406EY2OQA | openfda.unii |
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.