DIANEAL LOW CALCIUM WITH DEXTROSE
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
- DIANEAL LOW CALCIUM WITH DEXTROSE
- Generic name
- SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE
- Manufacturer
- Vantive US Healthcare LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b2b780d3-26ac-4e7c-a0f2-78991bee32a8
- SPL ID
- 348e5f59-47cf-e98e-e063-6394a90a33cd
- Version
- 4
- Effective date
- 2025-05-07
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:38
| Harmonized routes |
|---|
| INTRAPERITONEAL |
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 | DIANEAL LOW CALCIUM WITH DEXTROSE | openfda.brand_name | |
| generic name | SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE | openfda.generic_name | |
| manufacturer name | Vantive US Healthcare LLC | openfda.manufacturer_name | |
| ndc | package | 0941-0713-06 | openfda.package_ndc |
| ndc | package | 0941-0715-06 | openfda.package_ndc |
| ndc | package | 0941-0715-01 | openfda.package_ndc |
| ndc | package | 0941-0711-01 | openfda.package_ndc |
| ndc | package | 0941-0711-06 | openfda.package_ndc |
| ndc | package | 0941-0713-01 | openfda.package_ndc |
| ndc | product | 0941-0711 | openfda.product_ndc |
| ndc | product | 0941-0713 | openfda.product_ndc |
| ndc | product | 0941-0715 | openfda.product_ndc |
| ndc11 | package | 00941071506 | derived:openfda.package_ndc |
| ndc11 | package | 00941071101 | derived:openfda.package_ndc |
| ndc11 | package | 00941071501 | derived:openfda.package_ndc |
| ndc11 | package | 00941071301 | derived:openfda.package_ndc |
| ndc11 | package | 00941071106 | derived:openfda.package_ndc |
| ndc11 | package | 00941071306 | derived:openfda.package_ndc |
| rxcui | 800472 | openfda.rxcui | |
| rxcui | 800074 | openfda.rxcui | |
| rxcui | 800115 | openfda.rxcui | |
| rxcui | 800111 | openfda.rxcui | |
| rxcui | 800066 | openfda.rxcui | |
| rxcui | 800474 | openfda.rxcui | |
| spl id | 348e5f59-47cf-e98e-e063-6394a90a33cd | id | |
| spl set id | b2b780d3-26ac-4e7c-a0f2-78991bee32a8 | set_id | |
| unii | 02F3473H9O | openfda.unii | |
| unii | TU7HW0W0QT | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | M4I0D6VV5M | openfda.unii | |
| unii | LX22YL083G | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.