POTHOS FOETIDUS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Symplocarpus Foetidus Root.
Product ID | 15631-0356_140ee4a6-5373-47e2-a1e8-2f3ed54bb3fb |
NDC | 15631-0356 |
Product Type | Human Otc Drug |
Proprietary Name | POTHOS FOETIDUS |
Generic Name | Pothos Foetidus |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2015-09-12 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
Substance Name | SYMPLOCARPUS FOETIDUS ROOT |
Active Ingredient Strength | 1 [hp_X]/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2015-09-12 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-12 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-12 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-12 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-12 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-12 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-09-12 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
SYMPLOCARPUS FOETIDUS ROOT | 1 [hp_X]/1 |
SPL SET ID: | 1fe6bac9-2d00-4976-8f5d-735fb37324af |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
15631-0356 | POTHOS FOETIDUS | POTHOS FOETIDUS |
15631-0660 | POTHOS FOETIDUS | POTHOS FOETIDUS |