TINNITUS RELIEF (HOMEOLAB USA INC.)


Welcome to the PulseAid listing for the TINNITUS RELIEF drug offered from HOMEOLAB USA INC.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: HOMEOLAB USA INC.
NON-PROPRIETARY NAME: KALIUM BROMATUM, NUX VOMICA, CHINA RUBRA, SULPHUR, SANGUINARIA CANADENSIS, DULCAMARA, HYDRASTIS CANADENSIS, ARNICA MONTANA, BRYONIA ALBA, CAUSTICUM
SUBSTANCE NAME: POTASSIUM BROMIDE; STRYCHNOS NUX-VOMICA SEED; CINCHONA OFFICINALIS BARK; SULFUR; SANGUINARIA CANADENSIS ROOT; SOLANUM DULCAMARA STEM; GOLDENSEAL; ARNICA MONTANA; BRYONIA ALBA ROOT; CAUSTICUM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2013-10-18
END MARKETING DATE: 0000-00-00


TINNITUS RELIEF HUMAN OTC DRUG Details:

Item DescriptionTINNITUS RELIEF from HOMEOLAB USA INC.
LABELER NAME: HOMEOLAB USA INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 4; 4; 4; 4; 3; 3; 4; 4; 6([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2013-10-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-9054_cbb42dcc-3ad3-42be-89f8-64942e5ffab2
PRODUCT NDC: 60512-9054
APPLICATION NUMBER:

Other POTASSIUM BROMIDE; STRYCHNOS NUX-VOMICA SEED; CINCHONA OFFICINALIS BARK; SULFUR; SANGUINARIA CANADENSIS ROOT; SOLANUM DULCAMARA STEM; GOLDENSEAL; ARNICA MONTANA; BRYONIA ALBA ROOT; CAUSTICUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INC.TINNITUS RELIEF