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Arnicare
Arnicare - 0220-9000-54 - (ARNICA MONTANA)
Drug Information of Arnicare
| Product NDC: | 0220-9000 |
| Proprietary Name: | Arnicare |
| Non Proprietary Name: | ARNICA MONTANA |
| Active Ingredient(s): | 1 [hp_X]/g & nbsp; ARNICA MONTANA |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnicare
| Product NDC: | 0220-9000 |
| Labeler Name: | Laboratoires Boiron |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20070109 |
Package Information of Arnicare
| Package NDC: | 0220-9000-54 |
| Package Description: | 1 TUBE in 1 PACKAGE (0220-9000-54) > 45 g in 1 TUBE |
NDC Information of Arnicare
| NDC Code | 0220-9000-54 |
| Proprietary Name | Arnicare |
| Package Description | 1 TUBE in 1 PACKAGE (0220-9000-54) > 45 g in 1 TUBE |
| Product NDC | 0220-9000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20070109 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Laboratoires Boiron |
| Substance Name | ARNICA MONTANA |
| Strength Number | 1 |
| Strength Unit | [hp_X]/g |
| Pharmaceutical Classes |
