TINNITUS - 60512-6032-0 - (KALI BROMATUM, CINCHONA OFFICINALIS, SULPHUR, DULCAMARA, HYDRASTIS CANADENSIS, ARNICA MONTANA, BRYONIA CAUSTICUM)

Alphabetical Index


Drug Information of TINNITUS

Product NDC: 60512-6032
Proprietary Name: TINNITUS
Non Proprietary Name: KALI BROMATUM, CINCHONA OFFICINALIS, SULPHUR, DULCAMARA, HYDRASTIS CANADENSIS, ARNICA MONTANA, BRYONIA CAUSTICUM
Active Ingredient(s): 8; 8; 8; 8; 8; 8; 8; 8    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   KALI BROMATUM, CINCHONA OFFICINALIS, SULPHUR, DULCAMARA, HYDRASTIS CANADENSIS, ARNICA MONTANA, BRYONIA CAUSTICUM
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of TINNITUS

Product NDC: 60512-6032
Labeler Name: HOMEOLAB USA INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121025

Package Information of TINNITUS

Package NDC: 60512-6032-0
Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6032-0)

NDC Information of TINNITUS

NDC Code 60512-6032-0
Proprietary Name TINNITUS
Package Description 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6032-0)
Product NDC 60512-6032
Product Type Name HUMAN OTC DRUG
Non Proprietary Name KALI BROMATUM, CINCHONA OFFICINALIS, SULPHUR, DULCAMARA, HYDRASTIS CANADENSIS, ARNICA MONTANA, BRYONIA CAUSTICUM
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20121025
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name HOMEOLAB USA INC
Substance Name ARNICA MONTANA; BRYONIA ALBA ROOT; CAUSTICUM; CINCHONA OFFICINALIS BARK; GOLDENSEAL; POTASSIUM BROMIDE; SOLANUM DULCAMARA TOP; SULFUR
Strength Number 8; 8; 8; 8; 8; 8; 8; 8
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of TINNITUS


General Information