Product NDC: | 50845-0130 |
Proprietary Name: | Tinnitus Control |
Non Proprietary Name: | Arnica montana, Chininum sulphuricum, Ferrum metallicum, Kali phosphoricum, Natrum sulphuricum, Pulsatilla, Silicea, Thiosinaminum, |
Active Ingredient(s): | 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 & nbsp; Arnica montana, Chininum sulphuricum, Ferrum metallicum, Kali phosphoricum, Natrum sulphuricum, Pulsatilla, Silicea, Thiosinaminum, |
Administration Route(s): | ORAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50845-0130 |
Labeler Name: | Liddell Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20110426 |
Package NDC: | 50845-0130-1 |
Package Description: | 30 mL in 1 BOTTLE, SPRAY (50845-0130-1) |
NDC Code | 50845-0130-1 |
Proprietary Name | Tinnitus Control |
Package Description | 30 mL in 1 BOTTLE, SPRAY (50845-0130-1) |
Product NDC | 50845-0130 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Arnica montana, Chininum sulphuricum, Ferrum metallicum, Kali phosphoricum, Natrum sulphuricum, Pulsatilla, Silicea, Thiosinaminum, |
Dosage Form Name | SPRAY |
Route Name | ORAL |
Start Marketing Date | 20110426 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Liddell Laboratories, Inc. |
Substance Name | ALLYLTHIOUREA; ARNICA MONTANA; IRON; POTASSIUM PHOSPHATE, DIBASIC; PULSATILLA VULGARIS; QUININE SULFATE; SILICON DIOXIDE; SODIUM SULFATE |
Strength Number | 30; 30; 30; 30; 30; 30; 30; 30 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |