Chestal Adult Pellets
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 Adult Pellets
- Generic name
- ANTIMONY POTASSIUM TARTRATE,BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA WHOLE, IPECAC, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, PULSATILLA VULGARIS WHOLE, LOBARIA PULMONARIA
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a84e27cd-8e21-0fce-e053-2a95a90af2cf
- SPL ID
- 1136761e-f7a8-a719-e063-6294a90aebc3
- Version
- 6
- Effective date
- 2024-02-12
- Source export date
- 2026-11-06
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:46:06
| 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 Adult Pellets | openfda.brand_name | |
| generic name | ANTIMONY POTASSIUM TARTRATE,BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA WHOLE, IPECAC, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, PULSATILLA VULGARIS WHOLE, LOBARIA PULMONARIA | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9065-42 | openfda.package_ndc |
| ndc | package | 0220-9065-41 | openfda.package_ndc |
| ndc | product | 0220-9065 | openfda.product_ndc |
| ndc11 | package | 00220906541 | derived:openfda.package_ndc |
| ndc11 | package | 00220906542 | derived:openfda.package_ndc |
| spl id | 1136761e-f7a8-a719-e063-6294a90aebc3 | id | |
| spl set id | a84e27cd-8e21-0fce-e053-2a95a90af2cf | set_id | |
| unii | QR44N9XPJQ | openfda.unii | |
| unii | LZB7TFX1LT | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | 9N1RM2S62C | 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.