warnings
Warnings Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Advanced Arnica Plus
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
- Advanced Arnica Plus
- Generic name
- ARNICA MONTANA, ARNICA RAD, BELLIS PERENNIS, BRYONIA, HYPERICUM PERFORATUM, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, PHYTOLACCA DECANDRA, RHUS TOX, AND RUTA GRAVEOLENS.
- Manufacturer
- King Bio Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 8f1bac20-8403-4a15-bc29-f3bb1fa3c60d
- SPL ID
- c9f3c66e-e00f-4e62-beb4-5f73c663a9d0
- Version
- 1
- Effective date
- 2026-03-04
- Source export date
- 2026-10-27
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:09:39
| 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 | Advanced Arnica Plus | openfda.brand_name | |
| generic name | ARNICA MONTANA, ARNICA RAD, BELLIS PERENNIS, BRYONIA, HYPERICUM PERFORATUM, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, PHYTOLACCA DECANDRA, RHUS TOX, AND RUTA GRAVEOLENS. | openfda.generic_name | |
| manufacturer name | King Bio Inc. | openfda.manufacturer_name | |
| ndc | package | 57955-9979-2 | openfda.package_ndc |
| ndc | product | 57955-9979 | openfda.product_ndc |
| ndc11 | package | 57955997902 | derived:openfda.package_ndc |
| spl id | c9f3c66e-e00f-4e62-beb4-5f73c663a9d0 | id | |
| spl set id | 8f1bac20-8403-4a15-bc29-f3bb1fa3c60d | set_id | |
| unii | 11E6VI8VEG | openfda.unii | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 2HU33I03UY | openfda.unii | |
| unii | N94C2U587S | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | 2BMD2GNA4V | openfda.unii | |
| unii | MUE8Y11327 | 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.