| Product NDC: | 61727-111 |
| Proprietary Name: | Arnica Relief |
| Non Proprietary Name: | Arnica Montana 30C |
| Active Ingredient(s): | 30 [hp_C]/1 & nbsp; Arnica Montana 30C |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61727-111 |
| Labeler Name: | Homeocare Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120706 |
| Package NDC: | 61727-111-10 |
| Package Description: | 100 TABLET in 1 BOTTLE (61727-111-10) |
| NDC Code | 61727-111-10 |
| Proprietary Name | Arnica Relief |
| Package Description | 100 TABLET in 1 BOTTLE (61727-111-10) |
| Product NDC | 61727-111 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Arnica Montana 30C |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120706 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Homeocare Laboratories |
| Substance Name | ARNICA MONTANA |
| Strength Number | 30 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |