Multi-Vitamin Drops with Fluoride and Iron
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
- Multi-Vitamin Drops with Fluoride and Iron
- Generic name
- VITAMIN A, ASCORBIC ACID, CHOLECALCIFEROL, ALPHA-TOCOPHEROL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN 5-PHOSPHATE SODIUM, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FERROUS SULFATE AND SODIUM FLUORIDE
- Manufacturer
- Method Pharmaceuticals, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d5609742-e456-4409-bca9-706b0ea90d35
- SPL ID
- 41b5d787-acb5-89e9-e063-6294a90aa957
- Version
- 11
- Effective date
- 2025-10-21
- Source export date
- 2026-09-28
- 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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:14
| 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 | Multi-Vitamin Drops with Fluoride and Iron | openfda.brand_name | |
| generic name | VITAMIN A, ASCORBIC ACID, CHOLECALCIFEROL, ALPHA-TOCOPHEROL ACETATE, THIAMINE HYDROCHLORIDE, RIBOFLAVIN 5-PHOSPHATE SODIUM, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FERROUS SULFATE AND SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Method Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 58657-327-50 | openfda.package_ndc |
| ndc | product | 58657-327 | openfda.product_ndc |
| ndc11 | package | 58657032750 | derived:openfda.package_ndc |
| spl id | 41b5d787-acb5-89e9-e063-6294a90aa957 | id | |
| spl set id | d5609742-e456-4409-bca9-706b0ea90d35 | set_id | |
| unii | 39R4TAN1VT | openfda.unii | |
| unii | 25X51I8RD4 | openfda.unii | |
| unii | 1D1K0N0VVC | openfda.unii | |
| unii | 8ZYQ1474W7 | openfda.unii | |
| unii | 20RD1DZH99 | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | LU4B53JYVE | openfda.unii | |
| unii | M572600E5P | 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 S As in the case of all medications, keep out of reach of children.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Allergic rash and other idiosyncrasies have been rarely reported.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.