Tinnitus Control is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Liddell Laboratories, Inc.. The primary component is Arnica Montana; Quinine Sulfate; Iron; Potassium Phosphate, Dibasic; Sodium Sulfate; Pulsatilla Vulgaris; Silicon Dioxide; Allylthiourea.
| Product ID | 50845-0130_acecfee9-b0aa-4d83-84ba-a60aa6d9ad88 |
| NDC | 50845-0130 |
| Product Type | Human Otc Drug |
| Proprietary Name | Tinnitus Control |
| Generic Name | Arnica Montana, Chininum Sulphuricum, Ferrum Metallicum, Kali Phosphoricum, Natrum Sulphuricum, Pulsatilla, Silicea, Thiosinaminum, |
| Dosage Form | Spray |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-04-26 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Liddell Laboratories, Inc. |
| Substance Name | ARNICA MONTANA; QUININE SULFATE; IRON; POTASSIUM PHOSPHATE, DIBASIC; SODIUM SULFATE; PULSATILLA VULGARIS; SILICON DIOXIDE; ALLYLTHIOUREA |
| Active Ingredient Strength | 30 [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 | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2011-04-26 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-04-26 |
| Inactivation Date | 2019-10-29 |
| Ingredient | Strength |
|---|---|
| ARNICA MONTANA | 30 [hp_X]/mL |
| SPL SET ID: | a617e58b-1793-401d-b1ec-d419932ff897 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 43695-0009 | TINNITUS CONTROL | NOT APPLICABLE |
| 50845-0130 | Tinnitus Control | Arnica montana, Chininum sulphuricum, Ferrum metallicum, Kali phosphoricum, Natrum sulphuricum, Pulsatilla, Silicea, Thiosinaminum, |