| Product NDC: | 65111-002 |
| Proprietary Name: | Arnica Montana |
| Non Proprietary Name: | Arnica Montana |
| Active Ingredient(s): | 30 [hp_X]/1 & nbsp; Arnica Montana |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65111-002 |
| Labeler Name: | VITAMEDICA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19991201 |
| Package NDC: | 65111-002-74 |
| Package Description: | 250 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65111-002-74) |
| NDC Code | 65111-002-74 |
| Proprietary Name | Arnica Montana |
| Package Description | 250 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65111-002-74) |
| Product NDC | 65111-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Arnica Montana |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 19991201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | VITAMEDICA INC |
| Substance Name | ARNICA MONTANA |
| Strength Number | 30 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |