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 Description | TINNITUS RELIEF from HOMEOLAB USA INC. |
LABELER NAME: | HOMEOLAB USA INC. |
DEA SCHEDULE: |
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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: