Label: RING RELIEF- arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea - tablet, orally disintegrating
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Contains inactivated NDC Code(s)
NDC Code(s): 17312-015-14 - 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 January 17, 2020
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active Ingredients Purpose Arnica montana HPUS 6X, 30X Buzzing Hepar sulphuris calcareum HPUS 13X Sensitivity to Noise Hypericum perforatum HPUS 6X, 30X Nerve Sensitivity Lycopodium clavatum HPUS 12X Congestion, Throbbing Mercurius solubilis HPUS 13X Pain, Discomfort Salicylicum acidum HPUS 6X Ringing, Buzzing Silicea HPUS 13X Roaring Thiosinaminum HPUS 6X Ringing The letters HPUS indicate that the components of this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
- PURPOSE
- Uses
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Warnings
USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN.
- This product is intended to complement, not replace, standard medical treatment.
- Initial worsening of symptoms may occur.
- A physician should always be consulted to rule out serious causes.
- 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.
- If symptoms last longer than 7 days.
- Keep out of reach of children
- PREGNANCY OR BREAST FEEDING
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Directions
- Suitable for adults and children 12 years and above.
- 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.
- Children under the age of 12: consult a physician before use.
- Other information
- Inactive Ingredients
- Do not use if tamper evident seal is torn, broken or missing.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RING RELIEF
arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea - tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-015 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 6 [hp_X] CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 13 [hp_X] HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 6 [hp_X] LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 12 [hp_X] MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 13 [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 13 [hp_X] ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7) ALLYLTHIOUREA 6 [hp_X] Inactive Ingredients Ingredient Name Strength 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 Color white Score no score Shape DIAMOND Size 13mm Flavor Imprint Code TRP Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-015-14 1 in 1 PACKAGE 10/23/2012 1 70 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/01/2011 Labeler - TRP Company (105185719)