Santoninum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Santonin.
| Product ID | 71919-609_4836327c-0068-4d76-b5f9-06d5b5d093bc |
| NDC | 71919-609 |
| Product Type | Human Otc Drug |
| Proprietary Name | Santoninum |
| Generic Name | Santonin |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-03-16 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Washington Homeopathic Products |
| Substance Name | SANTONIN |
| Active Ingredient Strength | 30 [hp_C]/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2010-03-16 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-16 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-16 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-16 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-16 |
| Ingredient | Strength |
|---|---|
| SANTONIN | 30 [hp_C]/mL |
| SPL SET ID: | c803691a-15a3-465a-a5a9-380a67569174 |
| Manufacturer | |
| UNII | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0220-4558 | Santoninum | SANTONIN |
| 15631-0390 | SANTONINUM | SANTONINUM |
| 68428-622 | Santoninum | SANTONIN |
| 71919-609 | Santoninum | SANTONIN |