warnings
Warnings For external use only. Avoid contact with eyes and broken skin.
Arniflora
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
- Arniflora
- Generic name
- ARNICA MONTANA
- Manufacturer
- Schwabe North America, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 935bf19d-a32c-49b8-a5cc-13e7ddfb23fe
- SPL ID
- 62116d15-5876-4b4e-9d0b-c48b6a28fd71
- Version
- 15
- Effective date
- 2025-11-21
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:38:20
| Harmonized routes |
|---|
| TOPICAL |
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 | Arniflora | openfda.brand_name | |
| generic name | ARNICA MONTANA | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc | openfda.manufacturer_name | |
| ndc | package | 53499-5090-4 | openfda.package_ndc |
| ndc | package | 53499-5090-8 | openfda.package_ndc |
| ndc | product | 53499-5090 | openfda.product_ndc |
| ndc11 | package | 53499509004 | derived:openfda.package_ndc |
| ndc11 | package | 53499509008 | derived:openfda.package_ndc |
| spl id | 62116d15-5876-4b4e-9d0b-c48b6a28fd71 | id | |
| spl set id | 935bf19d-a32c-49b8-a5cc-13e7ddfb23fe | 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.