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 Supreme D
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 Supreme D
- Generic name
- ASCORBIC ACID, CHOLECALCIFEROL, ALPHA-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, FOLIC ACID, COBALAMIN, BIOTIN, PANTOTHENIC ACID, ZINC, SELENIUM
- Manufacturer
- Hillestad Pharmaceuticals USA
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 46fc3acf-1e6d-4830-ae9a-abd9c1132fca
- SPL ID
- e4c39ddd-ac1c-48f2-8251-6b6fe4f570a9
- Version
- 9
- Effective date
- 2026-01-27
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:32:27
| 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 Supreme D | openfda.brand_name | |
| generic name | ASCORBIC ACID, CHOLECALCIFEROL, ALPHA-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, FOLIC ACID, COBALAMIN, BIOTIN, PANTOTHENIC ACID, ZINC, SELENIUM | openfda.generic_name | |
| manufacturer name | Hillestad Pharmaceuticals USA | openfda.manufacturer_name | |
| ndc | package | 10542-009-02 | openfda.package_ndc |
| ndc | package | 10542-009-09 | openfda.package_ndc |
| ndc | product | 10542-009 | openfda.product_ndc |
| ndc11 | package | 10542000909 | derived:openfda.package_ndc |
| ndc11 | package | 10542000902 | derived:openfda.package_ndc |
| spl id | e4c39ddd-ac1c-48f2-8251-6b6fe4f570a9 | id | |
| spl set id | 46fc3acf-1e6d-4830-ae9a-abd9c1132fca | set_id | |
| unii | 25X51I8RD4 | openfda.unii | |
| unii | TLM2976OFR | openfda.unii | |
| unii | 935E97BOY8 | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | 0CH9049VIS | openfda.unii | |
| unii | LU4B53JYVE | openfda.unii | |
| unii | 568ET80C3D | openfda.unii | |
| unii | 6SO6U10H04 | openfda.unii | |
| unii | 8K0I04919X | openfda.unii | |
| unii | 68Y4CF58BV | openfda.unii | |
| unii | K72I3DEX9B | openfda.unii | |
| unii | 8406EY2OQA | openfda.unii | |
| unii | 1C6V77QF41 | 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.