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Arnica
Arnica - 50114-8000-8 - (ARNICA MONTANA ROOT)
Drug Information of Arnica
| Product NDC: | 50114-8000 |
| Proprietary Name: | Arnica |
| Non Proprietary Name: | ARNICA MONTANA ROOT |
| Active Ingredient(s): | 3 [hp_X]/50g & nbsp; ARNICA MONTANA ROOT |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnica
| Product NDC: | 50114-8000 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19900131 |
Package Information of Arnica
| Package NDC: | 50114-8000-8 |
| Package Description: | 1 TUBE in 1 CARTON (50114-8000-8) > 50 g in 1 TUBE |
NDC Information of Arnica
| NDC Code | 50114-8000-8 |
| Proprietary Name | Arnica |
| Package Description | 1 TUBE in 1 CARTON (50114-8000-8) > 50 g in 1 TUBE |
| Product NDC | 50114-8000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA ROOT |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19900131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | ARNICA MONTANA ROOT |
| Strength Number | 3 |
| Strength Unit | [hp_X]/50g |
| Pharmaceutical Classes |
