Sodium Chloride
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
- Sodium Chloride
- Generic name
- SODIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corporation
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 93aeac13-41de-4452-9f38-d6b4f38ada30
- SPL ID
- db478972-6e08-47d1-841c-92b4051a0527
- Version
- 4
- Effective date
- 2025-01-24
- Source export date
- 2026-11-06
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:54:48
| Harmonized routes |
|---|
| INTRAVENOUS |
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 | Sodium Chloride | openfda.brand_name | |
| generic name | SODIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Baxter Healthcare Corporation | openfda.manufacturer_name | |
| ndc | package | 0338-9793-12 | openfda.package_ndc |
| ndc | package | 0338-9791-01 | openfda.package_ndc |
| ndc | package | 0338-9808-24 | openfda.package_ndc |
| ndc | package | 0338-9791-40 | openfda.package_ndc |
| ndc | package | 0338-9808-01 | openfda.package_ndc |
| ndc | package | 0338-9793-01 | openfda.package_ndc |
| ndc | product | 0338-9793 | openfda.product_ndc |
| ndc | product | 0338-9791 | openfda.product_ndc |
| ndc | product | 0338-9808 | openfda.product_ndc |
| ndc11 | package | 00338979312 | derived:openfda.package_ndc |
| ndc11 | package | 00338980824 | derived:openfda.package_ndc |
| ndc11 | package | 00338979301 | derived:openfda.package_ndc |
| ndc11 | package | 00338979140 | derived:openfda.package_ndc |
| ndc11 | package | 00338979101 | derived:openfda.package_ndc |
| ndc11 | package | 00338980801 | derived:openfda.package_ndc |
| rxcui | 1807639 | openfda.rxcui | |
| rxcui | 1807634 | openfda.rxcui | |
| rxcui | 1807633 | openfda.rxcui | |
| spl id | db478972-6e08-47d1-841c-92b4051a0527 | id | |
| spl set id | 93aeac13-41de-4452-9f38-d6b4f38ada30 | set_id | |
| unii | 451W47IQ8X | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.