Nosebleed Relief (King Bio Inc.)


Welcome to the PulseAid listing for the Nosebleed Relief drug offered from King Bio 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: King Bio Inc.
NON-PROPRIETARY NAME: Ambrosia artemisiaefolia, Arnica montana, Bovista, Bryonia, Carbo vegetabilis, Ferrum Phosporicum, Hamamelis virginian, Ipecacuanha, Mercurius vivus, Nitricum acidum, Phosphorus, Trillium pendulum
SUBSTANCE NAME: AMBROSIA ARTEMISIIFOLIA; ARNICA MONTANA; LYCOPERDON UTRIFORME FRUITING BODY; BRYONIA ALBA ROOT; ACTIVATED CHARCOAL; FERROSOFERRIC PHOSPHATE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; IPECAC; MERCURY;
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-10-18
END MARKETING DATE: 0000-00-00


Nosebleed Relief HUMAN OTC DRUG Details:

Item DescriptionNosebleed Relief from King Bio Inc.
LABELER NAME: King Bio Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10([hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL)
START MARKETING DATE: 2012-10-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57955-0140_9a2d103e-6261-457a-b69f-e302e1d47ebd
PRODUCT NDC: 57955-0140
APPLICATION NUMBER:

Other AMBROSIA ARTEMISIIFOLIA; ARNICA MONTANA; LYCOPERDON UTRIFORME FRUITING BODY; BRYONIA ALBA ROOT; ACTIVATED CHARCOAL; FERROSOFERRIC PHOSPHATE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; IPECAC; MERCURY; Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
King Bio Inc.Nosebleed Relief