| Product NDC: | 10191-1255 |
| Proprietary Name: | ARNICA MONTANA (Whole Plant) |
| Non Proprietary Name: | ARNICA WHOLE PLANT |
| Active Ingredient(s): | 20 [hp_M]/1 & nbsp; ARNICA WHOLE PLANT |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10191-1255 |
| Labeler Name: | Remedy Makers |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20020821 |
| Package NDC: | 10191-1255-2 |
| Package Description: | 171 PELLET in 1 VIAL, GLASS (10191-1255-2) |
| NDC Code | 10191-1255-2 |
| Proprietary Name | ARNICA MONTANA (Whole Plant) |
| Package Description | 171 PELLET in 1 VIAL, GLASS (10191-1255-2) |
| Product NDC | 10191-1255 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA WHOLE PLANT |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20020821 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Remedy Makers |
| Substance Name | ARNICA MONTANA |
| Strength Number | 20 |
| Strength Unit | [hp_M]/1 |
| Pharmaceutical Classes |