DIARREX (Hyland’s)


Welcome to the PulseAid listing for the DIARREX drug offered from Hyland’s. 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: Hyland’s
NON-PROPRIETARY NAME: ARSENIC TRIOXIDE, PODOPHYLLUM, CHAMOMILE, PHOSPHORUS, and MERCURY
SUBSTANCE NAME: ARSENIC TRIOXIDE; PODOPHYLLUM; CHAMOMILE; PHOSPHORUS; MERCURY
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-05-17
END MARKETING DATE: 0000-00-00


DIARREX HUMAN OTC DRUG Details:

Item DescriptionDIARREX from Hyland’s
LABELER NAME: Hyland’s
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 6; 6; 6; 30([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2012-05-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54973-3134_55de479f-1216-4dc5-e054-00144ff88e88
PRODUCT NDC: 54973-3134
APPLICATION NUMBER:

Other ARSENIC TRIOXIDE; PODOPHYLLUM; CHAMOMILE; PHOSPHORUS; MERCURY Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hyland’sDIARREX