Allergy and Hay Fever (PharmWest Inc.)


Welcome to the PulseAid listing for the Allergy and Hay Fever drug offered from PharmWest 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: PharmWest Inc.
NON-PROPRIETARY NAME: Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Naphthalinum, Natrum muriaticum, Sabadilla, Wyethia helenioides
SUBSTANCE NAME: ONION; AMBROSIA ARTEMISIIFOLIA; ARSENIC TRIOXIDE; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; EUPHRASIA STRICTA; NAPHTHALENE; SODIUM CHLORIDE; SCHOENOCAULON OFFICINALE SEED; WYETHIA HELENIOIDES RO
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-11-08
END MARKETING DATE: 0000-00-00


Allergy and Hay Fever HUMAN OTC DRUG Details:

Item DescriptionAllergy and Hay Fever from PharmWest Inc.
LABELER NAME: PharmWest Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 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)
START MARKETING DATE: 2012-11-08
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50441-0002_7cdc345d-b78e-41dd-8d9d-7294f40f2966
PRODUCT NDC: 50441-0002
APPLICATION NUMBER:

Other ONION; AMBROSIA ARTEMISIIFOLIA; ARSENIC TRIOXIDE; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; EUPHRASIA STRICTA; NAPHTHALENE; SODIUM CHLORIDE; SCHOENOCAULON OFFICINALE SEED; WYETHIA HELENIOIDES RO Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
King Bio IncAllergy and Hay Fever Reliever
King Bio Inc.Allergy Hay Fever Reliever
PharmWest Inc.Allergy and Hay Fever