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
- 50fc30a0-0eca-452e-825e-08c2647ccfc1
- SPL ID
- 34a6a205-ce19-47ae-e063-6394a90acc12
- Version
- 4
- Effective date
- 2025-05-08
- Source export date
- 2026-10-12
- 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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:45:34
| 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 | |
| brand name | DIANEAL PD-2 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 | 0941-0698-01 | openfda.package_ndc |
| ndc | package | 0941-0696-06 | openfda.package_ndc |
| ndc | package | 0941-0696-01 | openfda.package_ndc |
| ndc | package | 0941-0698-06 | openfda.package_ndc |
| ndc | product | 0941-0696 | openfda.product_ndc |
| ndc | product | 0941-0698 | openfda.product_ndc |
| ndc11 | package | 00941069601 | derived:openfda.package_ndc |
| ndc11 | package | 00941069801 | derived:openfda.package_ndc |
| ndc11 | package | 00941069606 | derived:openfda.package_ndc |
| ndc11 | package | 00941069806 | derived:openfda.package_ndc |
| rxcui | 800074 | openfda.rxcui | |
| rxcui | 800066 | openfda.rxcui | |
| rxcui | 800062 | openfda.rxcui | |
| rxcui | 800064 | openfda.rxcui | |
| spl id | 34a6a205-ce19-47ae-e063-6394a90acc12 | id | |
| spl set id | 50fc30a0-0eca-452e-825e-08c2647ccfc1 | 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.