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Tinnitus Relief - 43689-0009-1 - (Calcarea Carbonica, Chininum Sulphuricum, Kali Carbonicum, Lycopodium Clavatum, Salicylicum Acidum)

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Drug Information of Tinnitus Relief

Product NDC: 43689-0009
Proprietary Name: Tinnitus Relief
Non Proprietary Name: Calcarea Carbonica, Chininum Sulphuricum, Kali Carbonicum, Lycopodium Clavatum, Salicylicum Acidum
Active Ingredient(s): 6; 6; 6; 6; 6    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   Calcarea Carbonica, Chininum Sulphuricum, Kali Carbonicum, Lycopodium Clavatum, Salicylicum Acidum
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tinnitus Relief

Product NDC: 43689-0009
Labeler Name: The Magni Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120816

Package Information of Tinnitus Relief

Package NDC: 43689-0009-1
Package Description: 125 TABLET in 1 BOTTLE (43689-0009-1)

NDC Information of Tinnitus Relief

NDC Code 43689-0009-1
Proprietary Name Tinnitus Relief
Package Description 125 TABLET in 1 BOTTLE (43689-0009-1)
Product NDC 43689-0009
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Calcarea Carbonica, Chininum Sulphuricum, Kali Carbonicum, Lycopodium Clavatum, Salicylicum Acidum
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120816
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name The Magni Company
Substance Name LYCOPODIUM CLAVATUM SPORE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM CARBONATE; QUININE SULFATE; SALICYLIC ACID
Strength Number 6; 6; 6; 6; 6
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of Tinnitus Relief


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