TRIFOLIUM PRATENSE is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Trifolium Pratense Flower.
| Product ID | 71919-686_99c3a0a3-6536-1628-e053-2995a90aa25a |
| NDC | 71919-686 |
| Product Type | Human Otc Drug |
| Proprietary Name | TRIFOLIUM PRATENSE |
| Generic Name | Ttrifolium Pratense |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-05-17 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Washington Homeopathic Products |
| Substance Name | TRIFOLIUM PRATENSE FLOWER |
| Active Ingredient Strength | 30 [hp_C]/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2011-05-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-05-17 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-05-17 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-05-17 |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-05-17 |
| Ingredient | Strength |
|---|---|
| TRIFOLIUM PRATENSE FLOWER | 30 [hp_C]/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 15631-0446 | TRIFOLIUM PRATENSE | TRIFOLIUM PRATENSE |
| 68428-683 | Trifolium pratense | TRIFOLIUM PRATENSE FLOWER |
| 71919-686 | TRIFOLIUM PRATENSE | Ttrifolium pratense |
| 22840-1514 | Red Clover | Trifolium pratense |
| 22840-1515 | Red Clover | Trifolium pratense |
| 22840-1565 | Red Clover | Trifolium pratense |
| 22840-5506 | Red Clover | Trifolium pratense |