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
- 0fb30b7e-8e1b-49c7-afac-2d5c01b9ff45
- SPL ID
- 34be97f0-8259-2735-e063-6394a90ad5fe
- Version
- 4
- Effective date
- 2025-05-09
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:56:30
| 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 | 0941-0690-01 | openfda.package_ndc |
| ndc | package | 0941-0690-08 | openfda.package_ndc |
| ndc | package | 0941-0694-08 | openfda.package_ndc |
| ndc | package | 0941-0694-01 | openfda.package_ndc |
| ndc | package | 0941-0686-08 | openfda.package_ndc |
| ndc | package | 0941-0686-01 | openfda.package_ndc |
| ndc | product | 0941-0686 | openfda.product_ndc |
| ndc | product | 0941-0694 | openfda.product_ndc |
| ndc | product | 0941-0690 | openfda.product_ndc |
| ndc11 | package | 00941069001 | derived:openfda.package_ndc |
| ndc11 | package | 00941069008 | derived:openfda.package_ndc |
| ndc11 | package | 00941068601 | derived:openfda.package_ndc |
| ndc11 | package | 00941069408 | derived:openfda.package_ndc |
| ndc11 | package | 00941068608 | derived:openfda.package_ndc |
| ndc11 | package | 00941069401 | 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 | 34be97f0-8259-2735-e063-6394a90ad5fe | id | |
| spl set id | 0fb30b7e-8e1b-49c7-afac-2d5c01b9ff45 | 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.