Label: RING RELIEF- arnica montana, calcium sulfide, hypericum perforatum, lycopodium clavatum spore, thiosinaminum, mercurius solubilis, salicylic acid, silicon dioxide, allylthiourea liquid
- NDC Code(s): 17312-001-11, 17312-001-15
- 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 March 5, 2024
If you are a consumer or patient please visit this version.
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ACTIVE INGREDIENT
Arnica montana HPUS 6x, 30x
Hepar sulph calc HPUS 13x
Hypericum perforatum HPUS 6x, 30x
Lycopodium clavatum HPUS 12x
Mercurius sol HPUS 13x
Salicylicum acidum HPUS 6x
Silicea HPUS 13x
Thiosinaminum HPUS 6x"HPUS" indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.
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PURPOSE
Arnica montana HPUS - Buzzing, Chirping
Hepar sulph calc HPUS - Noise sensitivity
Hypericum perforatum HPUS - Nerve sensitivity
Lycopodium clavatum HPUS - Pounding, wax buildup
Mercurius sol HPUS - Discomfort
Salicylicum acidum HPUS - Ringing, Buzzing
Silicea HPUS - Roaring
Thiosinaminum HPUS - Ringing (Tinnitus) -
INDICATIONS & USAGE
Uses:*
According to homeopathic indications, these ingredients temporarily relieve Tinnitus symptoms such as: • Ringing • Buzzing • Roaring • Nerve and Noise Sensitivity • Pounding • Discomfort • Wax buildup after serious causes have been ruled out by a physician.
*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. - ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- DO NOT USE
- Keep out of reach of children
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions:
Suitable for adults and children ages 2 and over.
• Children under the age of 2: consult a physician before use.
• For use in ear only.
• Use 3 to 5 drops twice per day or as needed.
• Warm contents to body temperature by holding in your hands. Tilt your head to the side and let solution drip into the ear. Never put the tip into the ear canal.
• Keep drops in your ear by tilting your head for 20-40 seconds.
Homeopathic remedies may not be effective for everyone.
May take up to 60 days to see results. -
SPL UNCLASSIFIED SECTION
Other information:
There are no known contraindications. Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects. Store in a cool dark location. Ring Relief® Ear Drops are homeopathic dilutions, for details see www.thereliefproducts.com. - INACTIVE INGREDIENT
- Questions or comments?
- Stop Use
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RING RELIEF
arnica montana, calcium sulfide, hypericum perforatum, lycopodium clavatum spore, thiosinaminum, mercurius solubilis, salicylic acid, silicon dioxide, allylthiourea liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-001 Route of Administration AURICULAR (OTIC) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 6 [hp_X] in 1 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 13 [hp_X] in 1 mL HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 6 [hp_X] in 1 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 12 [hp_X] in 1 mL MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 13 [hp_X] in 1 mL SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 6 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 13 [hp_X] in 1 mL ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7) ALLYLTHIOUREA 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-001-11 1 in 1 PACKAGE 06/01/2006 02/16/2018 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:17312-001-15 1 in 1 PACKAGE 05/05/2015 2 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/01/2006 Labeler - TRP Company (105185719) Registrant - TRP Company (105185719)