Aconitum Ferox is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Aconitum Ferox Root.
Product ID | 68428-176_6b1f3c4a-01ff-c60b-e053-2a91aa0a67de |
NDC | 68428-176 |
Product Type | Human Otc Drug |
Proprietary Name | Aconitum Ferox |
Generic Name | Aconitum Ferox Root |
Dosage Form | Pellet |
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]/1 |
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 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-01-26 |
Ingredient | Strength |
---|---|
ACONITUM FEROX ROOT | 30 [hp_C]/1 |
SPL SET ID: | 15393586-7cb8-4564-b815-47dc9dbf0bd0 |
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 |