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Arnicare Arnica
Arnicare Arnica - 0220-9059-04 - (ARNICA MONTANA)
Drug Information of Arnicare Arnica
| Product NDC: | 0220-9059 |
| Proprietary Name: | Arnicare Arnica |
| Non Proprietary Name: | ARNICA MONTANA |
| Active Ingredient(s): | 9 [hp_C]/1 & nbsp; ARNICA MONTANA |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnicare Arnica
| Product NDC: | 0220-9059 |
| Labeler Name: | Laboratoires Boiron |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110711 |
Package Information of Arnicare Arnica
| Package NDC: | 0220-9059-04 |
| Package Description: | 60 TABLET in 1 BLISTER PACK (0220-9059-04) |
NDC Information of Arnicare Arnica
| NDC Code | 0220-9059-04 |
| Proprietary Name | Arnicare Arnica |
| Package Description | 60 TABLET in 1 BLISTER PACK (0220-9059-04) |
| Product NDC | 0220-9059 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110711 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Laboratoires Boiron |
| Substance Name | ARNICA MONTANA |
| Strength Number | 9 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
