Boostervite
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
- Boostervite
- Generic name
- MULTIVITAMIN
- Manufacturer
- PureTek Corporation
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 53efbf65-8844-8486-e063-6394a90a51d3
- SPL ID
- 53efb4bb-24d4-8c55-e063-6394a90ab7b7
- Version
- 1
- Effective date
- 2026-06-18
- 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 05:26:40
| 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 | Boostervite | openfda.brand_name | |
| generic name | MULTIVITAMIN | openfda.generic_name | |
| manufacturer name | PureTek Corporation | openfda.manufacturer_name | |
| ndc | package | 59088-022-54 | openfda.package_ndc |
| ndc | product | 59088-022 | openfda.product_ndc |
| ndc11 | package | 59088002254 | derived:openfda.package_ndc |
| spl id | 53efb4bb-24d4-8c55-e063-6394a90ab7b7 | id | |
| spl set id | 53efbf65-8844-8486-e063-6394a90a51d3 | set_id | |
| unii | BR1SN1JS2W | openfda.unii | |
| unii | 5A9KE2L9L3 | openfda.unii | |
| unii | 19F5HK2737 | openfda.unii | |
| unii | 25X51I8RD4 | openfda.unii | |
| unii | R5L488RY0Q | openfda.unii | |
| unii | V038D626IF | openfda.unii | |
| unii | TLM2976OFR | openfda.unii | |
| unii | 128UH9LOAE | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | A9R10K3F2F | openfda.unii | |
| unii | 6SO6U10H04 | openfda.unii | |
| unii | 0Y3L4J38H1 | openfda.unii | |
| unii | 8K0I04919X | openfda.unii | |
| unii | 1L29G6428X | openfda.unii | |
| unii | 68Y4CF58BV | openfda.unii | |
| unii | 1C6V77QF41 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNING: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of reach of children. In case of accidental overdose, call a doctor or poison control center immediately. Administration of folate alone is improper therapy for pernicious anemia and other megaloblastic anemias in which vitamin B12 is deficient.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reactions: Allergic sensitization and other hypersensitivity reactions have been reported with oral folate supplementation. Ferrous Fumarate: Gastrointestinal disturbances, including anorexia, nausea, diarrhea, and constipation, have been reported. These effects are generally mild and may resolve with continued use. Administration of Boostervite™ with food may reduce the occurrence of gastrointestinal disturbances, although iron absorption may be decreased when taken with meals. Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein. However, allergic and idiosyncratic reactions are possible at lower levels. Iron, even at the usual recommended levels, has been associated with gastrointestinal intolerance in some patients. Call your healthcare provider for medical advice about side effects. You may report side effects to PureTek Corporation at 1-877-921-7873 . You may also report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.