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

Ring Relief by

Drug Labeling and Warnings

Ring Relief by is a Homeopathic medication manufactured, distributed, or labeled by TRP Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 diagnosis by a physician.

*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS

Warnings:
USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN AND UNDER THE SUPERVISION OF 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.

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.
• If symptoms last longer than 7 days.

DOSAGE & ADMINISTRATION

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.
• Homeopathic remedies may not be effective for everyone.
• May take up to 60 days to see results.
• Children under the age of 12: consult a physician before use.

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

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17312-043
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: 17312-043-14	1 in 1 PACKAGE	06/22/2015
1		50 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		06/22/2015

Labeler - TRP Company (105185719)

Registrant - TRP Company (105185719)