Tinnitus HP is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Ginkgo; Quinine Sulfate; Cinchona Officinalis Bark; Graphite; Sodium Salicylate; Lead; Salicylic Acid; Spigelia Anthelmia; Allylthiourea.
| Product ID | 44911-0078_4eb510d8-9c2b-48b4-b9ea-b51f5589b98e |
| NDC | 44911-0078 |
| Product Type | Human Otc Drug |
| Proprietary Name | Tinnitus HP |
| Generic Name | Ginkgo Biloba, Chininum Sulphuricum, Cinchona Officinalis, Graphites, Natrum Salicylicum, Plumbum Metallicum |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2013-04-12 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Energique, Inc. |
| Substance Name | GINKGO; QUININE SULFATE; CINCHONA OFFICINALIS BARK; GRAPHITE; SODIUM SALICYLATE; LEAD; SALICYLIC ACID; SPIGELIA ANTHELMIA; ALLYLTHIOUREA |
| Active Ingredient Strength | 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2013-04-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-04-12 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| GINKGO | 6 [hp_X]/mL |
| SPL SET ID: | 216a4307-ddc5-4ec8-82c1-56c4bd9d1bdb |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 57520-0306 | Tinnitus HP | Tinnitus HP |
| 44911-0078 | Tinnitus | Ginkgo Biloba, Chininum Sulphuricum, Cinchona Officinalis, Graphites, Natrum Salicylicum, Plumbum Metallicum |