Arnicare Arthritis
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 Arthritis
- Generic name
- ARNICA MONTANA, BENZOIC ACID, BRYONIA ALBA ROOT, MATRICARIA RECUTITA, SOLANUM DULCAMARA TOP, POTASSIUM IODIDE, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF
- Manufacturer
- Laboratoires Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cb02378b-617d-4268-b565-4136e50009f4
- SPL ID
- 57227ad0-b164-d600-e063-6294a90a64fa
- Version
- 12
- Effective date
- 2026-07-21
- Source export date
- 2026-10-27
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:07:31
| 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 Arthritis | openfda.brand_name | |
| generic name | ARNICA MONTANA, BENZOIC ACID, BRYONIA ALBA ROOT, MATRICARIA RECUTITA, SOLANUM DULCAMARA TOP, POTASSIUM IODIDE, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF | openfda.generic_name | |
| manufacturer name | Laboratoires Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-9044-29 | openfda.package_ndc |
| ndc | package | 0220-9044-04 | openfda.package_ndc |
| ndc | package | 0220-9044-92 | openfda.package_ndc |
| ndc | product | 0220-9044 | openfda.product_ndc |
| ndc11 | package | 00220904429 | derived:openfda.package_ndc |
| ndc11 | package | 00220904404 | derived:openfda.package_ndc |
| ndc11 | package | 00220904492 | derived:openfda.package_ndc |
| spl id | 57227ad0-b164-d600-e063-6294a90a64fa | id | |
| spl set id | cb02378b-617d-4268-b565-4136e50009f4 | set_id | |
| unii | KPS1B1162N | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 8SKN0B0MIM | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | IV92NQJ73U | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | 1C4QK22F9J | openfda.unii | |
| unii | G0R4UBI2ZZ | openfda.unii | |
| unii | I76KB35JEV | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.