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
- 0956bd7c-d46f-483a-bf2c-9e11c6111ebf
- SPL ID
- 38f81b8c-e9ff-2e12-e063-6394a90aac6f
- Version
- 6
- Effective date
- 2025-07-02
- Source export date
- 2026-10-27
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:59:15
| 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 | 0941-0735-01 | openfda.package_ndc |
| ndc | package | 0941-0733-04 | openfda.package_ndc |
| ndc | package | 0941-0733-01 | openfda.package_ndc |
| ndc | package | 0941-0735-04 | openfda.package_ndc |
| ndc | product | 0941-0733 | openfda.product_ndc |
| ndc | product | 0941-0735 | openfda.product_ndc |
| ndc11 | package | 00941073504 | derived:openfda.package_ndc |
| ndc11 | package | 00941073301 | derived:openfda.package_ndc |
| ndc11 | package | 00941073304 | derived:openfda.package_ndc |
| ndc11 | package | 00941073501 | derived:openfda.package_ndc |
| rxcui | 800472 | openfda.rxcui | |
| rxcui | 800115 | openfda.rxcui | |
| rxcui | 800111 | openfda.rxcui | |
| rxcui | 800474 | openfda.rxcui | |
| spl id | 38f81b8c-e9ff-2e12-e063-6394a90aac6f | id | |
| spl set id | 0956bd7c-d46f-483a-bf2c-9e11c6111ebf | 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.