| NDC Code: |
17312-003 |
| Proprietary Name: |
Ring Relief |
| Suffix: |
|
| Non-Proprietary Name: |
Potassium Sulfate, Salicylic Acid, Silicon Dioxide, Calcium Sulfate Anhydrous, Quinine Sulfate, Allylthiourea |
| Dosage Form: |
TABLET, MULTILAYER |
| Method: |
ORAL |
| Original Marketing Date: |
01-06-2006 |
| Category Name: |
UNAPPROVED HOMEOPATHIC |
| Application Number: |
|
| Labeler: |
TRP COMPANY |
| Substance Name: |
ALLYLTHIOUREA; ASCORBIC ACID; BIOTIN; CALCIUM SULFATE ANHYDROUS; CITRUS BIOFLAVONOIDS; CYANOCOBALAMIN; FOLIC ACID; GINKGO; INOSITOL; NIACINAMIDE; PANTOTHENIC ACID; POTASSIUM SULFATE; PYRIDOXINE; QUININE SULFATE; RIBOFLAVIN; SALICYLIC ACID; SILICON DIOXIDE; THIAMINE; ZINC PICOLINATE |
| Active Numerator Strength: |
6; 150; 100; 6; 300; 200; 200; 30; 37.5; 10; 2.5; 6; .5; 12; .5; 6; 6; .5; 7.5 |
| Active Ingredient Unit: |
[hp_X]/1; mg/1; ug/1; [hp_X]/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; [hp_X]/1; mg/1; [hp_X]/1; mg/1; [hp_X]/1; [hp_X]/1; mg/1; mg/1 |
| Pharm Classes: |
|
| DEA Schedule: |
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