| Product NDC: | 50048-138 |
| Proprietary Name: | Arnica Complex |
| Non Proprietary Name: | Arnica Montana |
| Active Ingredient(s): | 6 [hp_X]/1 & nbsp; Arnica Montana |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50048-138 |
| Labeler Name: | W Last CC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20091111 |
| Package NDC: | 50048-138-25 |
| Package Description: | 200 TABLET in 1 BOTTLE (50048-138-25) |
| NDC Code | 50048-138-25 |
| Proprietary Name | Arnica Complex |
| Package Description | 200 TABLET in 1 BOTTLE (50048-138-25) |
| Product NDC | 50048-138 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Arnica Montana |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091111 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | W Last CC |
| Substance Name | ARNICA MONTANA |
| Strength Number | 6 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |