Product NDC: | 44911-0078 |
Proprietary Name: | Tinnitus |
Non Proprietary Name: | Ginkgo Biloba, Chininum Sulphuricum, Cinchona Officinalis, Graphites, Natrum Salicylicum, Plumbum Metallicum |
Active Ingredient(s): | 30; 30; 6; 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; [hp_X]/mL & nbsp; Ginkgo Biloba, Chininum Sulphuricum, Cinchona Officinalis, Graphites, Natrum Salicylicum, Plumbum Metallicum |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44911-0078 |
Labeler Name: | Energique, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130412 |
Package NDC: | 44911-0078-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (44911-0078-1) |
NDC Code | 44911-0078-1 |
Proprietary Name | Tinnitus |
Package Description | 30 mL in 1 BOTTLE, DROPPER (44911-0078-1) |
Product NDC | 44911-0078 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ginkgo Biloba, Chininum Sulphuricum, Cinchona Officinalis, Graphites, Natrum Salicylicum, Plumbum Metallicum |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130412 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Energique, Inc. |
Substance Name | ALLYLTHIOUREA; CINCHONA OFFICINALIS BARK; GINKGO; GRAPHITE; LEAD; QUININE SULFATE; SALICYLIC ACID; SODIUM SALICYLATE; SPIGELIA ANTHELMIA |
Strength Number | 30; 30; 6; 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; [hp_X]/mL |
Pharmaceutical Classes |