GUNA-ALLERGY-PREV (Guna spa)


Welcome to the PulseAid listing for the GUNA-ALLERGY-PREV drug offered from Guna spa. 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: Guna spa
NON-PROPRIETARY NAME: AMBROSIA ARTEMISIIFOLIA – ANGUILLA ROSTRATA BLOOD SERUM – ARUNDO PLINIANA ROOT – BLACK CURRANT – CHELIDONIUM MAJUS – CITRIC ACID MONOHYDRATE – HISTAMINE DIHYDROCHLORIDE – HUMAN INTERLEUKIN 12 – INTERF
SUBSTANCE NAME: AMBROSIA ARTEMISIIFOLIA; ARUNDO PLINIANA ROOT; ASCLEPIAS CURASSAVICA; BLACK CURRANT; CITRIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; INTERFERON GAMMA-1B; HUMAN INTERLEUKIN 12; MANGANESE GLUCONATE;
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2006-05-23
END MARKETING DATE: 0000-00-00


GUNA-ALLERGY-PREV HUMAN OTC DRUG Details:

Item DescriptionGUNA-ALLERGY-PREV from Guna spa
LABELER NAME: Guna spa
DEA SCHEDULE:
ACTIVE STRENGTH: 18; 18; 6; 1; 6; 30; 4; 4; 4; 6; 200; 18; 18; 200; 6; 30; 18; 3; 18([hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X)
START MARKETING DATE: 2006-05-23
END MARKETING DATE: 0000-00-00
PRODUCT ID: 17089-299_8e14ec39-4a98-4fdf-b8d3-a9476a3e5370
PRODUCT NDC: 17089-299
APPLICATION NUMBER:

Other AMBROSIA ARTEMISIIFOLIA; ARUNDO PLINIANA ROOT; ASCLEPIAS CURASSAVICA; BLACK CURRANT; CITRIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; INTERFERON GAMMA-1B; HUMAN INTERLEUKIN 12; MANGANESE GLUCONATE; Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Guna spaGUNA-ALLERGY-PREV