Allergy D (Genexa LLC)


Welcome to the PulseAid listing for the Allergy D drug offered from Genexa LLC. 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: Genexa LLC
NON-PROPRIETARY NAME: Allium cepa, Ambrosia artemisiifolia, Arundo mauritanica, Dulcamara, Euphrasia officinalis, Nux vomica, Pulsatilla, Ranunculus bulbosus, Sabadilla, Sinapis nigra, Sticta pulmonaria, Wyethia helenoides
SUBSTANCE NAME: AMBROSIA ARTEMISIIFOLIA; STRYCHNOS NUX-VOMICA SEED; BLACK MUSTARD SEED; LOBARIA PULMONARIA; ARUNDO PLINIANA ROOT; RANUNCULUS BULBOSUS; PULSATILLA PRATENSIS; SCHOENOCAULON OFFICINALE SEED; SOLANUM DULC
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, CHEWABLE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2016-03-21
END MARKETING DATE: 0000-00-00


Allergy D HUMAN OTC DRUG Details:

Item DescriptionAllergy D from Genexa LLC
LABELER NAME: Genexa LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12([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: 2016-03-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69676-0071_4c712aa4-4425-37dd-e054-00144ff8d46c
PRODUCT NDC: 69676-0071
APPLICATION NUMBER:

Other AMBROSIA ARTEMISIIFOLIA; STRYCHNOS NUX-VOMICA SEED; BLACK MUSTARD SEED; LOBARIA PULMONARIA; ARUNDO PLINIANA ROOT; RANUNCULUS BULBOSUS; PULSATILLA PRATENSIS; SCHOENOCAULON OFFICINALE SEED; SOLANUM DULC Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genexa LLCAllergy D