Chestal
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
- Chestal
- Generic name
- ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA
- Manufacturer
- Laboratoires Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 76589f60-0f09-4d7a-8aaa-f1965df1fe9d
- SPL ID
- 05173f5f-6763-be69-e063-6394a90a8852
- Version
- 14
- Effective date
- 2023-09-11
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:56:26
| 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 |
|---|---|---|---|
| brand name | Chestal | openfda.brand_name | |
| generic name | ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA | openfda.generic_name | |
| manufacturer name | Laboratoires Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9032-16 | openfda.package_ndc |
| ndc | package | 0220-9032-28 | openfda.package_ndc |
| ndc | package | 0220-9032-15 | openfda.package_ndc |
| ndc | product | 0220-9032 | openfda.product_ndc |
| ndc11 | package | 00220903216 | derived:openfda.package_ndc |
| ndc11 | package | 00220903228 | derived:openfda.package_ndc |
| ndc11 | package | 00220903215 | derived:openfda.package_ndc |
| spl id | 05173f5f-6763-be69-e063-6394a90a8852 | id | |
| spl set id | 76589f60-0f09-4d7a-8aaa-f1965df1fe9d | set_id | |
| unii | LZB7TFX1LT | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | 9N1RM2S62C | openfda.unii | |
| unii | 75O014T1HG | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | 1PIP394IID | openfda.unii | |
| unii | I76KB35JEV | openfda.unii | |
| unii | D1YM0P5Z2T | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.