Multitrace -4 Pediatric
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
- Multitrace -4 Pediatric
- Generic name
- TRACE ELEMENTS 4
- Manufacturer
- American Regent, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 5ee6a685-3c35-467b-8d4d-79efdd0bfa8e
- SPL ID
- 8e5be3e5-1916-4d19-87ab-e2092f5d4c5a
- Version
- 4
- Effective date
- 2019-04-25
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:25
| Harmonized routes |
|---|
| INTRAVENOUS |
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 | Multitrace -4 Pediatric | openfda.brand_name | |
| generic name | TRACE ELEMENTS 4 | openfda.generic_name | |
| manufacturer name | American Regent, Inc. | openfda.manufacturer_name | |
| ndc | package | 0517-9203-25 | openfda.package_ndc |
| ndc | product | 0517-9203 | openfda.product_ndc |
| ndc11 | package | 00517920325 | derived:openfda.package_ndc |
| rxcui | 1293466 | openfda.rxcui | |
| rxcui | 1293464 | openfda.rxcui | |
| spl id | 8e5be3e5-1916-4d19-87ab-e2092f5d4c5a | id | |
| spl set id | 5ee6a685-3c35-467b-8d4d-79efdd0bfa8e | set_id | |
| unii | LRX7AJ16DT | openfda.unii | |
| unii | N57JI2K7WP | openfda.unii | |
| unii | W00LYS4T26 | openfda.unii | |
| unii | KB1PCR9DMW | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Copper and Manganese are eliminated via the bile. In patients with severe liver dysfunction and/or biliary tract obstruction, decreasing or omitting copper and manganese supplements entirely may be necessary. This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS The amounts of ZINC, COPPER, MANGANESE, AND CHROMIUM in the solution are very small and toxicity symptoms due to these trace elements at suggested dosage levels are considered unlikely to occur.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.