Product NDC: | 17312-001 |
Proprietary Name: | Ring Relief |
Non Proprietary Name: | Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea |
Active Ingredient(s): | 6; 6; 13; 6; 12; 13; 6; 13 [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, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea |
Administration Route(s): | AURICULAR (OTIC) |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17312-001 |
Labeler Name: | TRP Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20060601 |
Package NDC: | 17312-001-11 |
Package Description: | 1 BOTTLE, DROPPER in 1 PACKAGE (17312-001-11) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 17312-001-11 |
Proprietary Name | Ring Relief |
Package Description | 1 BOTTLE, DROPPER in 1 PACKAGE (17312-001-11) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 17312-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea |
Dosage Form Name | LIQUID |
Route Name | AURICULAR (OTIC) |
Start Marketing Date | 20060601 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | TRP Company |
Substance Name | ALLYLTHIOUREA; ARNICA MONTANA; CALCIUM SULFIDE; HYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; SALICYLIC ACID; SILICON DIOXIDE |
Strength Number | 6; 6; 13; 6; 12; 13; 6; 13 |
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 |