Label: RING RELIEF- arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea - tablet, orally disintegrating

  • 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

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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

  • 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.

  • WARNINGS

    Warnings:

    A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES.

    • 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.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • WARNINGS

    • In case of overdose, get medical help or contact a Poison Control Center right away.

    Stop use and ask a doctor if:

    • You experience ear pain or worsening symptoms.
    • Symptoms last longer than 7 days.
  • DOSAGE & ADMINISTRATION

    Directions

    • Suitable for adults and children ages 2 and over.
    • Children under the age of 2: Consult a physician before use.
    • Dissolve entire tablet under tongue.
    • Do not chew or swallow whole.
    • Take 1 tablet 3 times a day or as directed by a physician.
    • Use up to 6 times a day as needed.
    • Take at least 10 minutes before or at least 10 minutes after eating or drinking.
    • 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 Fast Disolving Tablets are homeopathic dilutions: see www.thereliefproducts.com for details.
  • INACTIVE INGREDIENT

    Inactive Ingredients
    Advantol® 300, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose.

  • Do not use if tamper evident seal is torn, broken or missing.

  • QUESTIONS

    Questions or comments? 888-969-6855
    www.thereliefproducts.com

  • PRINCIPAL DISPLAY PANEL

    CartonLabel

  • INGREDIENTS AND APPEARANCE
    RING RELIEF 
    arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea - tablet, orally disintegrating
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17312-023
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA6 [hp_X]
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE13 [hp_X]
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM6 [hp_X]
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE12 [hp_X]
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS13 [hp_X]
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID6 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE13 [hp_X]
    ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7) ALLYLTHIOUREA6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MANNITOL (UNII: 3OWL53L36A)  
    SORBITOL (UNII: 506T60A25R)  
    CROSPOVIDONE (UNII: 68401960MK)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    COPOVIDONE (UNII: D9C330MD8B)  
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeDIAMONDSize13mm
    FlavorImprint Code TRP
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17312-023-141 in 1 PACKAGE12/01/2011
    170 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/01/2011
    Labeler - TRP Company (105185719)
    Registrant - TRP Company (105185719)
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