PSORIASISREAL RELIEF (HOMEOLAB USA INC)


Welcome to the PulseAid listing for the PSORIASIS 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: SULPHUR, ARSENICUM ALBUM, ALUMEN, MAGNESIA SULPHURICUM, NATRUM SULPHURICUM
SUBSTANCE NAME: SULFUR; ARSENIC TRIOXIDE; POTASSIUM ALUM; MAGNESIUM SULFATE HEPTAHYDRATE; SODIUM SULFATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, CHEWABLE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-07-11
END MARKETING DATE: 0000-00-00


PSORIASIS REAL RELIEF HUMAN OTC DRUG Details:

Item DescriptionPSORIASIS REAL RELIEF from HOMEOLAB USA INC
LABELER NAME: HOMEOLAB USA INC
DEA SCHEDULE:
ACTIVE STRENGTH: 8; 8; 8; 8; 8([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2012-07-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-6010_7a89dc56-e0f8-474c-8db5-4c3b37464df5
PRODUCT NDC: 60512-6010
APPLICATION NUMBER:

Other SULFUR; ARSENIC TRIOXIDE; POTASSIUM ALUM; MAGNESIUM SULFATE HEPTAHYDRATE; SODIUM SULFATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INCPSORIASIS