GUNA-ALLERGY-PREV

Product NDC

17089-299

11-digit product format

170890299

Labeler code

17089

Product ID

17089-299_7e029048-a7aa-68a5-e053-2a91aa0af0be

Type

HUMAN OTC DRUG

Nonproprietary name

AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - 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 -

Dosage form

SOLUTION/ DROPS

Route

ORAL

Labeler

Guna spa

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2006-05-23

Substance

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 strength

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; g/30mL; [hp_X]/30mL

Pharmacologic classes

Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Interferon gamma [EPC], Interferon-gamma [CS], Magnetic Resonance Contrast Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes