DIAMITE (HOMEOLAB USA INC)


Welcome to the PulseAid listing for the DIAMITE 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 FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, N
SUBSTANCE NAME: CALCIUM FLUORIDE; CALCIUM PHOSPHATE; CALCIUM SULFATE; FERRUM PHOSPHORICUM; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; SODIUM PH
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, CHEWABLE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2014-03-28
END MARKETING DATE: 0000-00-00


DIAMITE HUMAN OTC DRUG Details:

Item DescriptionDIAMITE from HOMEOLAB USA INC
LABELER NAME: HOMEOLAB USA INC
DEA SCHEDULE:
ACTIVE STRENGTH: 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 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; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2014-03-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 60512-8035_336b7627-d812-449a-883b-a59c92992a0b
PRODUCT NDC: 60512-8035
APPLICATION NUMBER:

Other CALCIUM FLUORIDE; CALCIUM PHOSPHATE; CALCIUM SULFATE; FERRUM PHOSPHORICUM; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; SODIUM PH Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
HOMEOLAB USA INCDIAMITE