Overview
Arnica montana flower is a plant/plant extract used in some OTC (over-the-counter) products. It is not an approved drug.
Indication
No indication information available.
Associated Conditions
- Phlebitis superficial
- Swelling
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2022/03/17 | Phase 2 | UNKNOWN | |||
2020/12/21 | Phase 4 | Completed | Endo Pharmaceuticals | ||
2020/09/01 | Phase 4 | Completed | |||
2018/05/11 | Not Applicable | Completed | |||
2012/05/15 | Not Applicable | Completed | Wynand BWH Melenhorst, MD | ||
2008/10/17 | Phase 4 | Completed | |||
2006/08/15 | Not Applicable | Completed | |||
2005/09/22 | Phase 3 | Terminated | University Hospital, Grenoble |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Nutritional Specialties, Inc. | 83027-0036 | ORAL | 6 [hp_X] in 1 mL | 4/14/2025 | |
| VITAMEDICA, INC. | 80004-005 | ORAL | 30 [hp_X] in 1 1 | 5/5/2025 | |
| King Bio Inc. | 57955-2822 | ORAL | 10 [hp_X] in 59 mL | 5/20/2025 | |
| King Bio Inc. | 57955-2803 | ORAL | 10 [hp_X] in 59 mL | 5/20/2025 | |
| Vsf2 Inc. | 86100-0016 | ORAL | 10 [hp_X] in 59 mL | 9/9/2025 | |
| Grove Acquisition Subsidiary, Inc. dba VitaMedica | 80004-005 | ORAL | 30 [hp_X] in 1 1 | 4/8/2025 | |
| VITAMEDICA, INC. | 80004-005 | ORAL | 30 [hp_X] in 1 1 | 4/8/2025 | |
| Deseret Biologicals, Inc. | 43742-2246 | ORAL | 4 [hp_X] in 1 mL | 5/27/2025 | |
| Uriel Pharmacy, Inc | 48951-1406 | TOPICAL | 3 [hp_X] in 1 g | 9/8/2025 | |
| King Bio Inc. | 57955-5276 | ORAL | 10 [hp_X] in 59 mL | 5/19/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| HEEL 020 TAB | 01969471 | Tablet - Oral | 4 D / TAB | 12/31/1992 | |
| ARNICA MONTANA GRANULE 1DH - 30CH | dolisos laboratoires s.a. | 00699691 | Tablet - Oral | 1 DH / DH | 12/31/1987 |
| HP16 DPS | 01975803 | Drops - Oral | 200 X / ML | 10/4/1996 | |
| ARNICA PWR 4X | koegler laboratories inc. | 00858269 | Powder - Oral | 4 X / X | 12/31/1989 |
| RHM-DORON 102A - DROPS | weleda ag heilmittelbetriebe | 02174200 | Drops
,
Liquid - Oral | 3 D / ML | 4/9/1998 |
| ARNICA COMP - CREAM | 02176777 | Cream - Topical | 3 D / G | 4/14/1998 | |
| LPCC COMP - DROPS | weleda ag heilmittelbetriebe | 02174162 | Liquid
,
Drops - Oral | 3 D / ML | 4/9/1998 |
| TRAUMEEL HEEL-082 TAB | 01969498 | Tablet - Oral | 2 DH / TAB | 12/31/1992 | |
| A-B COMPOSITUM - LIQ | weleda ag heilmittelbetriebe | 02110539 | Liquid - Oral | 20 D / ML | 12/31/1995 |
| ACONITUM COMPOSE SOLUTE | dolisos laboratoires s.a. | 00719455 | Drops - Oral | 3 CH / CH | 12/31/1988 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
Help Us Improve
Your feedback helps us provide better drug information and insights.