Sabadilla Eucalyptus (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Sabadilla Eucalyptus 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: Sabadilla Eucalyptus
SUBSTANCE NAME: BRYONIA ALBA ROOT; EUCALYPTUS GUM; EUPATORIUM PERFOLIATUM FLOWERING TOP; ACONITUM NAPELLUS; SCHOENOCAULON OFFICINALE SEED; PHOSPHORUS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


Sabadilla Eucalyptus HUMAN OTC DRUG Details:

Item DescriptionSabadilla Eucalyptus from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 3; 3; 4; 4; 6([hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-8313_54c2a204-5434-15b5-e054-00144ff88e88
PRODUCT NDC: 48951-8313
APPLICATION NUMBER:

Other BRYONIA ALBA ROOT; EUCALYPTUS GUM; EUPATORIUM PERFOLIATUM FLOWERING TOP; ACONITUM NAPELLUS; SCHOENOCAULON OFFICINALE SEED; PHOSPHORUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Sabadilla Eucalyptus