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
- b79ef556-37b3-4fd0-8589-c633033be9df
- SPL ID
- 38f8e8b2-1f8a-e0aa-e063-6294a90ad63f
- Version
- 6
- Effective date
- 2025-07-02
- Source export date
- 2026-10-27
- 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/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:50:50
| 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 | 0941-0729-02 | openfda.package_ndc |
| ndc | package | 0941-0731-01 | openfda.package_ndc |
| ndc | package | 0941-0727-02 | openfda.package_ndc |
| ndc | package | 0941-0729-01 | openfda.package_ndc |
| ndc | package | 0941-0727-01 | openfda.package_ndc |
| ndc | package | 0941-0731-02 | openfda.package_ndc |
| ndc | product | 0941-0727 | openfda.product_ndc |
| ndc | product | 0941-0729 | openfda.product_ndc |
| ndc | product | 0941-0731 | openfda.product_ndc |
| ndc11 | package | 00941073102 | derived:openfda.package_ndc |
| ndc11 | package | 00941072701 | derived:openfda.package_ndc |
| ndc11 | package | 00941072702 | derived:openfda.package_ndc |
| ndc11 | package | 00941073101 | derived:openfda.package_ndc |
| ndc11 | package | 00941072902 | derived:openfda.package_ndc |
| ndc11 | package | 00941072901 | 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 | 38f8e8b2-1f8a-e0aa-e063-6294a90ad63f | id | |
| spl set id | b79ef556-37b3-4fd0-8589-c633033be9df | 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.