Tinnitus Control (Liddell Laboratories, Inc.)
Welcome to the PulseAid listing for the Tinnitus Control drug offered from Liddell Laboratories, Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Liddell Laboratories, Inc. |
| NON-PROPRIETARY NAME: | Arnica montana, Chininum sulphuricum, Ferrum metallicum, Kali phosphoricum, Natrum sulphuricum, Pulsatilla, Silicea, Thiosinaminum, |
| SUBSTANCE NAME: | ARNICA MONTANA; QUININE SULFATE; IRON; POTASSIUM PHOSPHATE, DIBASIC; SODIUM SULFATE; PULSATILLA VULGARIS; SILICON DIOXIDE; ALLYLTHIOUREA |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | SPRAY |
| MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
| START MARKETING DATE: | 2011-04-26 |
| END MARKETING DATE: | 0000-00-00 |
Tinnitus Control HUMAN OTC DRUG Details:
| Item Description | Tinnitus Control from Liddell Laboratories, Inc. |
| LABELER NAME: | Liddell Laboratories, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 30; 30; 30; 30; 30; 30; 30; 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) |
| START MARKETING DATE: | 2011-04-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50845-0130_acecfee9-b0aa-4d83-84ba-a60aa6d9ad88 |
| PRODUCT NDC: | 50845-0130 |
| APPLICATION NUMBER: | |
Other ARNICA MONTANA; QUININE SULFATE; IRON; POTASSIUM PHOSPHATE, DIBASIC; SODIUM SULFATE; PULSATILLA VULGARIS; SILICON DIOXIDE; ALLYLTHIOUREA Pharmaceutical Manufacturers / Labelers:
