TINNITUS RELIEF- calcarea carbonica, chininum sulphuricum, kali carbonicum, lycopodium clavatum, salicylicum acidum tablet

Tinnitus Relief by

Drug Labeling and Warnings

Tinnitus Relief by is a Homeopathic medication manufactured, distributed, or labeled by The Magni Company, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS: ​Calcarea Carbonica 6X, Chininum Sulphuricum 6X, Kali Carbonicum 6X, Lycopodium Clavatum 6X, Salicylicum Acidum 6X

PURPOSE

INDICATIONS:​Temporarily relieves noises in the ears due to history of exposure to loud noises such as,

ringining, buzzing, hissing, whistling, roaring.

WARNINGS

WARNINGS:​If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

DIRECTIONS:​Adults and children 12 years and above, Dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician.

Children under 12 years, consult a physician.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:​Lactose (Fast Flo Lactose USP 316), Magnesium Stearate, Microcrystalline Cellulose

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.

INDICATIONS & USAGE

INDICATIONS: Temporarily relieves noises in the ears due to history of exposure to loud noises such as,

ringining, buzzing, hissing, whistling, roaring.

QUESTIONS

Dist. by: The Magni Group, Inc. McKinney, TX 75071 USA

www.magnilife.com 1-800-645-9199

PRINCIPAL DISPLAY PANEL

MAGNILIFE Homeopathic

NDC: 43689-0009-1

TINNITUS RELIEF

For Ringining in the Ears

125 Tablets

INGREDIENTS AND APPEARANCE

TINNITUS RELIEF 
calcarea carbonica, chininum sulphuricum, kali carbonicum, lycopodium clavatum, salicylicum acidum tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43689-0009
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	6 [hp_X]
QUININE SULFATE (UNII: KF7Z0E0Q2B) (QUININE - UNII:A7V27PHC7A)	QUININE SULFATE	6 [hp_X]
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D)	POTASSIUM CARBONATE	6 [hp_X]
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	6 [hp_X]
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

Product Characteristics
Color	white	Score	no score
Shape	ROUND (Convex)	Size	6mm
Flavor		Imprint Code	ML
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43689-0009-1	125 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/16/2012

Labeler - The Magni Company (113501902)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43689-0009)