TINNITUS CONTROL - arnica montana, chininum sulphuricum, ferrum metallicum, kali phosphoricum, natrum sulphuricum, pulsatilla, s

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

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Active ingredient:
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW), QUININE SULFATE (UNII: KF7Z0E0Q2B) (QUININE - UNII:A7V27PHC7A), IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7), POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (POTASSIUM CATION - UNII:295O53K152), SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37), PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4), ALLYLTHIOUREA (UNII:
Available from:
Liddell Laboratories, Inc.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
INDICATIONS:   Helps relieve symptoms of Tinnitus. INDICATIONS:   Helps relieve symptoms of Tinnitus.
Authorization status:
unapproved homeopathic
Authorization number:
50845-0130-1

TINNITUS CONTROL - arnica montana, chininum sulphuricum, ferrum metallicum, kali

phosphoricum, natrum sulphuricum, pulsatilla, silicea, thiosinaminum, spray

Liddell Laboratories, Inc.

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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Tinnitus Control

ACTIVE INGREDIENTS: Arnica montana 30X, Chininum sulphuricum 30X, Ferrum Metallicum 30X,

Kali phosphoricum 30X, Natrum sulphuricum 30X, Pulsatilla 30X, Silicea 30X, Thiosinaminum 30X.

INDICATIONS: Helps relieve symptoms of Tinnitus.

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.

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

INDICATIONS: Helps relieve symptoms of Tinnitus.

Distributed by:

Nutralogy

2049 North Lincoln Street

Burbank, CA 91504

Made in the USA

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

Control Center right away.

Tinnitus Control

Helps relieve the symptoms of Tinnitus

HOMEOPATHIC

1.0 fl. oz. (30 ml)

TINNITUS CONTROL

arnica montana, chininum sulphuricum, ferrum metallicum, kali phosphoricum, natrum sulphuricum, pulsatilla,

silicea, thiosinaminum, spray

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:50 8 45-0 130

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

30 [hp_X]

in 1 mL

Q UININE SULFATE (UNII: KF7Z0 E0 Q2B) (QUININE - UNII:A7V27PHC7A)

QUININE SULFATE

30 [hp_X]

in 1 mL

IRO N (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7)

IRON

30 [hp_X]

in 1 mL

PO TASSIUM PHO SPHATE, DIBASIC (UNII: CI71S9 8 N1Z) (POTASSIUM CATION -

UNII:29 5O 53K152)

POTASSIUM PHOSPHATE,

DIBASIC

30 [hp_X]

in 1 mL

SO DIUM SULFATE (UNII: 0 YPR6 5R21J) (SODIUM CATION - UNII:LYR4M0 NH37)

SODIUM SULFATE

30 [hp_X]

in 1 mL

PULSATILLA VULGARIS (UNII: I76 KB35JEV) (PULSATILLA VULGARIS -

UNII:I76 KB35JEV)

PULSATILLA VULGARIS

30 [hp_X]

in 1 mL

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

SILICON DIOXIDE

30 [hp_X]

in 1 mL

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

ALLYLTHIOUREA

30 [hp_X]

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

ALCO HO L (UNII: 3K9 9 58 V9 0 M)

Liddell Laboratories, Inc.

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:50 8 45-0 130 -1

30 mL in 1 BOTTLE, SPRAY

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

0 4/26 /20 11

Labeler -

Liddell Laboratories, Inc. (832264241)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Liddell Labo rato ries, Inc.

8 3226 4241

ma nufa c ture

Revised: 4/2011

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