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GUNA-ALLERGY-PREV - AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERF

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Field Value
NDC Code: 17089-299
Proprietary Name: GUNA-ALLERGY-PREV
Suffix:
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
Dosage Form: SOLUTION/ DROPS
Method: ORAL
Original Marketing Date: 23-05-2006
Category Name: UNAPPROVED HOMEOPATHIC
Application Number:
Labeler: GUNA SPA
Substance Name: AMBROSIA ARTEMISIIFOLIA; ANGUILLA ROSTRATA BLOOD SERUM; ARUNDO PLINIANA ROOT; ASCLEPIAS CURASSAVICA; BLACK CURRANT; CITRIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; HUMAN INTERLEUKIN 12; INTERFERON GAMMA-1B; MANGANESE GLUCONATE; PARIETARIA OFFICINALIS; PHLEUM PRATENSE; SODIUM PYRUVATE; SODIUM SULFATE; SUCCINIC ACID; SULFUR; URTICA URENS; VIBURNUM OPULUS ROOT; WYETHIA HELENIOIDES ROOT
Active Numerator Strength: 18; 200; 18; 6; 1; 6; 30; 4; 4; 4; 18; 18; 6; 200; 6; 30; 18; 3; 18
Active Ingredient Unit: [hp_X]/30mL; [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]/30mL; mL/30mL; [hp_X]/30mL
Pharm Classes:
DEA Schedule: