warnings
Warnings Do not use this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor.
Arnica Montana 30C
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 30C
- Generic name
- ARNICA MONTANA
- Manufacturer
- Schwabe Mexico, S.A. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a4743dcd-dd86-4d56-9d61-3dfb60598076
- SPL ID
- cd693332-cf97-4139-a5df-0c7164f94730
- Version
- 7
- Effective date
- 2022-05-20
- Source export date
- 2026-10-12
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:29:10
| Harmonized routes |
|---|
| SUBLINGUAL |
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 30C | openfda.brand_name | |
| generic name | ARNICA MONTANA | openfda.generic_name | |
| manufacturer name | Schwabe Mexico, S.A. de C.V. | openfda.manufacturer_name | |
| ndc | package | 68466-1041-2 | openfda.package_ndc |
| ndc | product | 68466-1041 | openfda.product_ndc |
| ndc11 | package | 68466104102 | derived:openfda.package_ndc |
| spl id | cd693332-cf97-4139-a5df-0c7164f94730 | id | |
| spl set id | a4743dcd-dd86-4d56-9d61-3dfb60598076 | 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.