TINNITUSREAL RELIEF (HOMEOLAB USA INC)
Welcome to the PulseAid listing for the TINNITUS 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: | KALI BROMATUM, CINCHONA OFFICINALIS, SULPHUR, DULCAMARA, HYDRASTIS CANADENSIS, ARNICA MONTANA, BRYONIA CAUSTICUM |
| SUBSTANCE NAME: | POTASSIUM BROMIDE; CINCHONA OFFICINALIS BARK; SULFUR; SOLANUM DULCAMARA TOP; GOLDENSEAL; ARNICA MONTANA; BRYONIA ALBA ROOT; CAUSTICUM |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, CHEWABLE |
| MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
| START MARKETING DATE: | 2012-10-25 |
| END MARKETING DATE: | 0000-00-00 |
TINNITUS REAL RELIEF HUMAN OTC DRUG Details:
| Item Description | TINNITUS REAL RELIEF from HOMEOLAB USA INC |
| LABELER NAME: | HOMEOLAB USA INC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 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) |
| START MARKETING DATE: | 2012-10-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 60512-6032_59e5548e-a0dd-4cbc-92bf-718665cc26db |
| PRODUCT NDC: | 60512-6032 |
| APPLICATION NUMBER: | |
Other POTASSIUM BROMIDE; CINCHONA OFFICINALIS BARK; SULFUR; SOLANUM DULCAMARA TOP; GOLDENSEAL; ARNICA MONTANA; BRYONIA ALBA ROOT; CAUSTICUM Pharmaceutical Manufacturers / Labelers:
