Arnicare Leg Cramps
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
- Arnicare Leg Cramps
- Generic name
- ARNICA MONTANA WHOLE, COPPER, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA TOP, CLAVICEPS PURPUREA SCLEROTIUM
- Manufacturer
- Laboratoires Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 051a4e17-c665-ec4d-e063-6294a90aabe6
- SPL ID
- 570fbc3a-1c54-e0f6-e063-6394a90a6d25
- Version
- 5
- Effective date
- 2026-07-20
- Source export date
- 2026-09-28
- 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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:19
| 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 | Arnicare Leg Cramps | openfda.brand_name | |
| generic name | ARNICA MONTANA WHOLE, COPPER, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, STRYCHNOS NUX-VOMICA SEED, PASSIFLORA INCARNATA TOP, CLAVICEPS PURPUREA SCLEROTIUM | openfda.generic_name | |
| manufacturer name | Laboratoires Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9079-92 | openfda.package_ndc |
| ndc | package | 0220-9079-29 | openfda.package_ndc |
| ndc | package | 0220-9079-04 | openfda.package_ndc |
| ndc | product | 0220-9079 | openfda.product_ndc |
| ndc11 | package | 00220907929 | derived:openfda.package_ndc |
| ndc11 | package | 00220907904 | derived:openfda.package_ndc |
| ndc11 | package | 00220907992 | derived:openfda.package_ndc |
| spl id | 570fbc3a-1c54-e0f6-e063-6394a90a6d25 | id | |
| spl set id | 051a4e17-c665-ec4d-e063-6294a90aabe6 | set_id | |
| unii | 789U1901C5 | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | CLF5YFS11O | openfda.unii | |
| unii | 01G9XEA93N | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.