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GUNA-ALLERGY-PREV - 17089-299-18 - (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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Drug Information of GUNA-ALLERGY-PREV

Product NDC: 17089-299
Proprietary Name: GUNA-ALLERGY-PREV
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
Active Ingredient(s): 18; 200; 18; 6; 1; 6; 30; 4; 4; 4; 18; 18; 6; 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_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 & nbsp;   AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERF
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-ALLERGY-PREV

Product NDC: 17089-299
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060523

Package Information of GUNA-ALLERGY-PREV

Package NDC: 17089-299-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-299-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-ALLERGY-PREV

NDC Code 17089-299-18
Proprietary Name GUNA-ALLERGY-PREV
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-299-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-299
Product Type Name HUMAN OTC DRUG
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 Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20060523
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name 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
Strength Number 18; 200; 18; 6; 1; 6; 30; 4; 4; 4; 18; 18; 6; 200; 6; 30; 18; 3; 18
Strength 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
Pharmaceutical Classes

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