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.

  • 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.

  • 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

    Warnings:

    A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. For External Use Only.

    • This product is intended to complement, not replace, standard medical treatment.
    • Initial worsening of symptoms may occur.
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • DO NOT USE

    Do not use:

    • If solution changes color or becomes cloudy.
    • If you have ear drainage, discharge, irritation, a rash in the ear or dizziness.
    • If you have ear tubes, after surgery or with damaged ear drums.

  • Keep out of reach of children

  • WARNINGS

    • In case of accidental ingestion, get medical help or contact a Poison Control Center right away.
    • Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
  • 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

    Inactive Ingredients:
    Benzalkonium Chloride, Glycerin, Purified Water.

  • Questions or comments?

    www.thereliefproducts.com, 1-888-969-6855

  • Stop Use

    Stop use and ask a doctor if: • You experience ear pain or worsening symptoms. • Your symptoms last longer than 7 days.

  • PRINCIPAL DISPLAY PANEL

    Carton

    Label

  • INGREDIENTS AND APPEARANCE
    RING RELIEF 
    arnica montana, calcium sulfide, hypericum perforatum, lycopodium clavatum spore, thiosinaminum, mercurius solubilis, salicylic acid, silicon dioxide, allylthiourea liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17312-001
    Route of AdministrationAURICULAR (OTIC)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA6 [hp_X]  in 1 mL
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE13 [hp_X]  in 1 mL
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM6 [hp_X]  in 1 mL
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE12 [hp_X]  in 1 mL
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS13 [hp_X]  in 1 mL
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID6 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE13 [hp_X]  in 1 mL
    ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7) ALLYLTHIOUREA6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17312-001-111 in 1 PACKAGE06/01/200602/16/2018
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:17312-001-151 in 1 PACKAGE05/05/2015
    210 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/01/2006
    Labeler - TRP Company (105185719)
    Registrant - TRP Company (105185719)