FIBROMYALGIA RELIEF (HOMEOLAB USA INC.)


Welcome to the PulseAid listing for the FIBROMYALGIA 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: CALCAREA PHOSPHORICA, IGNATIA AMARA, CAUSTICUM, RHUS TOXICODENDRON, MAGNESIA PHOSPHORICA, BRYONIA ALBA, ARNICA MONTANA, HYPERICUM, CANTHARIS, KALI BICHROMICUM,
SUBSTANCE NAME: CALCIUM PHOSPHATE; STRYCHNOS IGNATII SEED; CAUSTICUM; TOXICODENDRON RADICANS LEAF; MAGNESIUM PHOSPHATE, DIBASIC; BRYONIA ALBA ROOT; ARNICA MONTANA; HYPERICUM PERFORATUM; LYTTA VESICATORIA; POTASSIUM D
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


FIBROMYALGIA RELIEF HUMAN OTC DRUG Details:

Item DescriptionFIBROMYALGIA RELIEF from HOMEOLAB USA INC.
LABELER NAME: HOMEOLAB USA INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 7; 9; 7; 7; 7; 7; 9; 9; 9; 9([hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1)
START MARKETING DATE: 2013-10-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-9056_5ab5a64f-b7b6-43df-81e8-c81badc6d214
PRODUCT NDC: 60512-9056
APPLICATION NUMBER:

Other CALCIUM PHOSPHATE; STRYCHNOS IGNATII SEED; CAUSTICUM; TOXICODENDRON RADICANS LEAF; MAGNESIUM PHOSPHATE, DIBASIC; BRYONIA ALBA ROOT; ARNICA MONTANA; HYPERICUM PERFORATUM; LYTTA VESICATORIA; POTASSIUM D Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INC.FIBROMYALGIA RELIEF