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Arnica
Arnica - 53645-1000-0 - (Arnica)
Drug Information of Arnica
| Product NDC: | 53645-1000 |
| Proprietary Name: | Arnica |
| Non Proprietary Name: | Arnica |
| Active Ingredient(s): | 6 [hp_X]/50mL & nbsp; Arnica |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnica
| Product NDC: | 53645-1000 |
| Labeler Name: | True Botanica, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20121113 |
Package Information of Arnica
| Package NDC: | 53645-1000-0 |
| Package Description: | 50 mL in 1 BOTTLE, WITH APPLICATOR (53645-1000-0) |
NDC Information of Arnica
| NDC Code | 53645-1000-0 |
| Proprietary Name | Arnica |
| Package Description | 50 mL in 1 BOTTLE, WITH APPLICATOR (53645-1000-0) |
| Product NDC | 53645-1000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Arnica |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121113 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | True Botanica, LLC |
| Substance Name | ARNICA MONTANA FLOWER |
| Strength Number | 6 |
| Strength Unit | [hp_X]/50mL |
| Pharmaceutical Classes |
