Potassium 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
- Potassium Chloride
- Generic name
- POTASSIUM CHLORIDE
- Manufacturer
- Guardian Drug Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 3d460e84-27a0-485c-8b11-58d03d9064aa
- SPL ID
- 859606e1-12d2-4eff-b6f3-4fa59c4da89b
- Version
- 3
- Effective date
- 2021-07-28
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:16:02
| Harmonized routes |
|---|
| ORAL |
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 |
|---|---|---|---|
| application applno | ANDA | 214892 | derived:openfda.application_number |
| application number | ANDA214892 | openfda.application_number | |
| brand name | Potassium Chloride | openfda.brand_name | |
| generic name | POTASSIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Guardian Drug Company | openfda.manufacturer_name | |
| ndc | package | 53041-680-06 | openfda.package_ndc |
| ndc | package | 53041-681-97 | openfda.package_ndc |
| ndc | package | 53041-681-17 | openfda.package_ndc |
| ndc | package | 53041-681-29 | openfda.package_ndc |
| ndc | package | 53041-681-06 | openfda.package_ndc |
| ndc | package | 53041-681-96 | openfda.package_ndc |
| ndc | product | 53041-680 | openfda.product_ndc |
| ndc | product | 53041-681 | openfda.product_ndc |
| ndc11 | package | 53041068197 | derived:openfda.package_ndc |
| ndc11 | package | 53041068006 | derived:openfda.package_ndc |
| ndc11 | package | 53041068129 | derived:openfda.package_ndc |
| ndc11 | package | 53041068196 | derived:openfda.package_ndc |
| ndc11 | package | 53041068117 | derived:openfda.package_ndc |
| ndc11 | package | 53041068106 | derived:openfda.package_ndc |
| rxcui | 314182 | openfda.rxcui | |
| rxcui | 312515 | openfda.rxcui | |
| spl id | 859606e1-12d2-4eff-b6f3-4fa59c4da89b | id | |
| spl set id | 3d460e84-27a0-485c-8b11-58d03d9064aa | set_id | |
| unii | 660YQ98I10 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS Gastrointestinal Irritation: Dilute before use, take with meals (5.1) 5.1 Gastrointestinal Irritation May cause gastrointestinal irritation if administered undiluted. Increased dilution of the solution and taking with meals may reduce gastrointestinal irritation [see Dosage and Administration (2.1)] .
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS The most common adverse reactions to oral potassium salts are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea. Most common adverse reactions are nausea, vomiting, flatulence, abdominal pain/discomfort, and diarrhea. (6) To report SUSPECTED ADVERSE REACTIONS, contact Guardian Drug Company at 609-860-2600 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.