Aconitum ferox is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Aconitum Ferox Root.
| Product ID | 71919-007_7e3e9fce-f2d1-8cc9-e053-2a91aa0aad73 |
| NDC | 71919-007 |
| Product Type | Human Otc Drug |
| Proprietary Name | Aconitum ferox |
| Generic Name | Aconitum Ferox Root |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-01-26 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Washington Homeopathic Products |
| Substance Name | ACONITUM FEROX ROOT |
| Active Ingredient Strength | 30 [hp_C]/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2011-01-26 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-01-26 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-01-26 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-01-26 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-01-26 |
| Ingredient | Strength |
|---|---|
| ACONITUM FEROX ROOT | 30 [hp_C]/mL |
| SPL SET ID: | e7c5005d-82b5-4824-ab25-acbefc415fce |
| Manufacturer | |
| UNII | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 60512-6442 | ACONITUM FEROX | ACONITUM FEROX |
| 68428-176 | Aconitum Ferox | ACONITUM FEROX ROOT |
| 71919-007 | Aconitum ferox | ACONITUM FEROX ROOT |