Silica (Uriel Pharmacy Inc)


Welcome to the PulseAid listing for the Silica drug offered from Uriel Pharmacy 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: Uriel Pharmacy Inc
NON-PROPRIETARY NAME: Silica
SUBSTANCE NAME: EQUISETUM ARVENSE TOP; WHITE OAK BARK; MAMMAL LIVER
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: POWDER
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


Silica HUMAN OTC DRUG Details:

Item DescriptionSilica from Uriel Pharmacy Inc
LABELER NAME: Uriel Pharmacy Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 9; 9([hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-8317_551153e9-cc50-5cb8-e054-00144ff88e88
PRODUCT NDC: 48951-8317
APPLICATION NUMBER:

Other EQUISETUM ARVENSE TOP; WHITE OAK BARK; MAMMAL LIVER Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy IncSilica