warnings
Do not use if you have an allergy or hypersensitivity to the components of the formula. more than the maximum daily dosage unless directed by a doctor.
Arnica Montana
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
- Arnica Montana
- Generic name
- ARNICA MONTANA
- Manufacturer
- NARTEX LABORATORIOS HOMEOPATICOS SA DE CV
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3c62d081-4178-4ac0-b81f-d97202dee8ea
- SPL ID
- 3c46848d-23e8-a387-e063-6394a90a83e8
- Version
- 9
- Effective date
- 2025-08-13
- Source export date
- 2026-10-12
- 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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:47:29
| 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 | Arnica Montana | openfda.brand_name | |
| generic name | ARNICA MONTANA | openfda.generic_name | |
| manufacturer name | NARTEX LABORATORIOS HOMEOPATICOS SA DE CV | openfda.manufacturer_name | |
| ndc | package | 34666-091-50 | openfda.package_ndc |
| ndc | product | 34666-091 | openfda.product_ndc |
| ndc11 | package | 34666009150 | derived:openfda.package_ndc |
| spl id | 3c46848d-23e8-a387-e063-6394a90a83e8 | id | |
| spl set id | 3c62d081-4178-4ac0-b81f-d97202dee8ea | set_id | |
| unii | O80TY208ZW | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.