TINNITUS CONTROL- arnica montana, chininum sulphuricum, ferrum metallicum, kali phosphoricum, natrum sulphuricum, pulsatilla, silicea, thiosinaminum, spray

Tinnitus Control by

Drug Labeling and Warnings

Tinnitus Control by is a Homeopathic medication manufactured, distributed, or labeled by Liddell Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:  Arnica montana 30X, Chininum sulphuricum 30X, Ferrum Metallicum 30X, Kali phosphoricum 30X, Natrum sulphuricum 30X, Pulsatilla 30X, Silicea 30X, Thiosinaminum 30X.

PURPOSE

INDICATIONS:  Helps relieve symptoms of Tinnitus.

WARNINGS

WARNINGS:  If pregnant or breast feeding, seek the advice of a doctor before use.

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal around neck of bottle is missing or broken.

DOSAGE & ADMINISTRATION

DIRECTIONS:  Adults and Children over 12:  Spray twice under the tongue 3 times per day.  Children under 12:  Consult a doctor prior to use.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:  Alcohol 20% v/v, Purified water.

INDICATIONS & USAGE

INDICATIONS:  Helps relieve symptoms of Tinnitus.

QUESTIONS

Distributed by:

Nutralogy

2049 North Lincoln Street

Burbank, CA 91504

Made in the USA

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

Tinnitus Control

Helps relieve the symptoms of Tinnitus

HOMEOPATHIC

1.0 fl. oz. (30 ml)

INGREDIENTS AND APPEARANCE

TINNITUS CONTROL 
arnica montana, chininum sulphuricum, ferrum metallicum, kali phosphoricum, natrum sulphuricum, pulsatilla, silicea, thiosinaminum, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50845-0130
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	30 [hp_X]  in 1 mL
QUININE SULFATE (UNII: KF7Z0E0Q2B) (QUININE - UNII:A7V27PHC7A)	QUININE SULFATE	30 [hp_X]  in 1 mL
IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7)	IRON	30 [hp_X]  in 1 mL
POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM PHOSPHATE, DIBASIC	30 [hp_X]  in 1 mL
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM SULFATE	30 [hp_X]  in 1 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	30 [hp_X]  in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	30 [hp_X]  in 1 mL
ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7)	ALLYLTHIOUREA	30 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50845-0130-1	30 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/26/2011

Labeler - Liddell Laboratories, Inc. (832264241)

Establishment
Name	Address	ID/FEI	Business Operations
Liddell Laboratories, Inc.		832264241	manufacture