Label: RING RELIEF- potassium sulfate, salicylic acid, silicon dioxide, calcium sulfate anhydrous, quinine sulfate, allylthiourea tablet, multilayer
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Contains inactivated NDC Code(s)
NDC Code(s): 17312-003-12 - Packager: TRP Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated May 31, 2012
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- Official Label (Printer Friendly)
- Homeopathic Purpose
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Active Ingredients
Kali Sulphuricum 6x Salicylicum Acidum 6x,12x Silicea 6x Calcarea Sulphuricum 6x Chininum Sulphuricum 12x Thiosinaminum 6x,12x Citrus Bioflavonoids 300 mg Ginkgo 30 mg Thiamine 0.5 mg Riboflavin 0.5 mg Niacinamide 10 mg Pantothenic Acid 2.5 mg Pyridoxine 0.5 mg Cyanocobalamin 200 mcg Biotin 100 mcg Folic Acid 200 mcg Inositol 37.5 mg Zinc Picolinate 7.5 mg Ascorbic Acid 150 mg - Inactive Ingredients
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Do not use
- Stop Use and See A Doctor If
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Directions
Take 1 caplet, morning and evening, 5 minutes before or 20 minutes after a meal. Let the homeopathic external shell dissolve in your mouth until the sweetness is gone (approx. 20-40 seconds), then swallow the remaining vitamin enriched core with water. For faster results take 1 caplet 3 times per day. For best results, use for at least 6 months. After desired results are achieved, reduce dosing to 1 caplet 2 times per day.
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Other Information
Tinnitus may be a symptom of a more serious health condition and your doctor should be consulted for proper diagnosis. Over the counter drugs like aspirin or drugs such as caffeine and tobacco can aggravate tinnitus. For maximum results, and especially if earwax build up is an issue, use caplets with Ring Relief Ear Drops.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RING RELIEF
potassium sulfate, salicylic acid, silicon dioxide, calcium sulfate anhydrous, quinine sulfate, allylthiourea tablet, multilayerProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-003 Route of Administration Oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Potassium Sulfate (UNII: 1K573LC5TV) (Potassium Cation - UNII:295O53K152) Potassium Sulfate 6 [hp_X] Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 6 [hp_X] Silicon Dioxide (UNII: ETJ7Z6XBU4) (Silicon Dioxide - UNII:ETJ7Z6XBU4) Silicon Dioxide 6 [hp_X] Calcium Sulfate Anhydrous (UNII: E934B3V59H) (Calcium Cation - UNII:2M83C4R6ZB) Calcium Sulfate Anhydrous 6 [hp_X] Quinine Sulfate (UNII: KF7Z0E0Q2B) (Quinine - UNII:A7V27PHC7A) Quinine Sulfate 12 [hp_X] Allylthiourea (UNII: 706IDJ14B7) (Allylthiourea - UNII:706IDJ14B7) Allylthiourea 6 [hp_X] Citrus Bioflavonoids (UNII: BD70459I50) (Citrus Bioflavonoids - UNII:BD70459I50) Citrus Bioflavonoids 300 mg Ginkgo (UNII: 19FUJ2C58T) (Ginkgo - UNII:19FUJ2C58T) Ginkgo 30 mg Thiamine (UNII: X66NSO3N35) (Thiamine - UNII:X66NSO3N35) Thiamine 0.5 mg Riboflavin (UNII: TLM2976OFR) (Riboflavin - UNII:TLM2976OFR) Riboflavin 0.5 mg Niacinamide (UNII: 25X51I8RD4) (Niacinamide - UNII:25X51I8RD4) Niacinamide 10 mg Pantothenic Acid (UNII: 19F5HK2737) (Pantothenic Acid - UNII:19F5HK2737) Pantothenic Acid 2.5 mg Pyridoxine (UNII: KV2JZ1BI6Z) (Pyridoxine - UNII:KV2JZ1BI6Z) Pyridoxine 0.5 mg Cyanocobalamin (UNII: P6YC3EG204) (Cyanocobalamin - UNII:P6YC3EG204) Cyanocobalamin 200 ug Biotin (UNII: 6SO6U10H04) (Biotin - UNII:6SO6U10H04) Biotin 100 ug Folic Acid (UNII: 935E97BOY8) (Folic Acid - UNII:935E97BOY8) Folic Acid 200 ug Inositol (UNII: 4L6452S749) (Inositol - UNII:4L6452S749) Inositol 37.5 mg Zinc Picolinate (UNII: ALO92O31SE) (Zinc Picolinate - UNII:ALO92O31SE) Zinc Picolinate 7.5 mg Ascorbic Acid (UNII: PQ6CK8PD0R) (Ascorbic Acid - UNII:PQ6CK8PD0R) Ascorbic Acid 150 mg Inactive Ingredients Ingredient Name Strength Sucrose (UNII: C151H8M554) Lactose (UNII: J2B2A4N98G) Cellulose, Microcrystalline (UNII: OP1R32D61U) Stearic Acid (UNII: 4ELV7Z65AP) Croscarmellose Sodium (UNII: M28OL1HH48) Silicon Dioxide (UNII: ETJ7Z6XBU4) Magnesium Stearate (UNII: 70097M6I30) Sucralose (UNII: 96K6UQ3ZD4) Product Characteristics Color white Score no score Shape OVAL (Tablet) Size 9mm Flavor Imprint Code None Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-003-12 1 in 1 Package 1 60 in 1 Bottle Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/01/2006 Labeler - TRP Company (105185719)
