RING RELIEF- arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicyl

United States - English - NLM (National Library of Medicine)

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Active ingredient:
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW), CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q), HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB), LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479), MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2), SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SIL
Available from:
TRP Company
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
According to homeopathic indications, these ingredients temporarily relieve multi symptoms of: • Ringing, Buzzing, Roaring • Nerve & Noise Sensitivity • Congestion • Throbbing • Pain & Discomfort and eardrum problems after diagnosis by a physician.
Authorization status:
unapproved homeopathic
Authorization number:
17312-015-14

RING RELIEF- arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum

spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea - tablet, orally

disintegrating

TRP Company

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.

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Ring Relief Homeopathic Fast Dissolving Tablets

Active Ingredients

Purpos e

Arnica montana HPUS

6X, 30X

Buzzing

Hepar sulphuris calcareum HPUS 13X

Sensitivity to Noise

Hypericum perforatum HPUS

6X, 30X

Nerve Sensitivity

Lycopodium clavatum HPUS

Congestion, Throbbing

Mercurius solubilis HPUS

Pain, Discomfort

Salicylicum acidum HPUS

Ringing, Buzzing

Silicea HPUS

Roaring

Thiosinaminum HPUS

Ringing

The letters HPUS indicate that the components of this product are officially monographed in the

Homeopathic Pharmacopoeia of the United States.

Us es

According to homeopathic indications, these ingredients temporarily relieve multi symptoms of:

Ringing, Buzzing, Roaring Nerve & Noise Sensitivity Congestion Throbbing Pain & Discomfort

and eardrum problems after diagnosis by a physician.

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

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

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

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.

Inactive Ingredients

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

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

For more information and to order related products call toll free: 888-969-6855 or trpcompany.com

RING RELIEF

arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis -

salicylic acid - silicon dioxide - allylthiourea - tablet, orally disintegrating

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:17312-0 15

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ARNICA MO NTANA (UNII: O8 0 TY20 8 ZW) (ARNICA MONTANA - UNII:O8 0 TY20 8 ZW)

ARNICA MONTANA

6 [hp_X]

CALCIUM SULFIDE (UNII: 1MBW0 7J51Q) (CALCIUM SULFIDE - UNII:1MBW0 7J51Q)

CALCIUM SULFIDE

13 [hp_X]

HYPERICUM PERFO RATUM (UNII: XK4IUX8 MNB) (HYPERICUM PERFORATUM -

UNII:XK4IUX8 MNB)

HYPERICUM PERFORATUM 6 [hp_X]

TRP Company

LYCO PO DIUM CLAVATUM SPO RE (UNII: C8 8 X29 Y479 ) (LYCOPODIUM CLAVATUM

SPORE - UNII:C8 8 X29 Y479 )

LYCOPODIUM CLAVATUM

SPORE

12 [hp_X]

MERCURIUS SO LUBILIS (UNII: 324Y40 38 G2) (MERCURIUS SOLUBILIS -

UNII:324Y40 38 G2)

MERCURIUS SOLUBILIS

13 [hp_X]

SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)

SALICYLIC ACID

6 [hp_X]

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6 XBU4)

SILICON DIOXIDE

13 [hp_X]

ALLYLTHIO UREA (UNII: 70 6 IDJ14B7) (ALLYLTHIOUREA - UNII:70 6 IDJ14B7)

ALLYLTHIOUREA

6 [hp_X]

Inactive Ingredients

Ingredient Name

Stre ng th

MANNITO L (UNII: 3OWL53L36 A)

SO RBITO L (UNII: 50 6 T6 0 A25R)

CRO SPO VIDO NE (UNII: 6 8 40 19 6 0 MK)

CELLULO SE, MICRO CRYSTALLINE (UNII: OP1R32D6 1U)

CO PO VIDO NE (UNII: D9 C330 MD8 B)

LACTO SE (UNII: J2B2A4N9 8 G)

MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 )

Product Characteristics

Color

white

S core

no sco re

S hap e

DIAMOND

S iz e

13mm

Flavor

Imprint Code

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:17312-0 15-14

1 in 1 PACKAGE

10 /23/20 12

1

70 in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

12/0 1/20 11

Labeler -

T RP Company (105185719)

Revised: 1/2020

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