NDC 17089-299

GUNA-ALLERGY-PREV

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 -

GUNA-ALLERGY-PREV is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Ambrosia Artemisiifolia; Arundo Pliniana Root; Asclepias Curassavica; Black Currant; Citric Acid Monohydrate; Histamine Dihydrochloride; Interferon Gamma-1b; Human Interleukin 12; Manganese Gluconate; Sodium Pyruvate; Sodium Sulfate; Parietaria Officinalis; Phleum Pratense; Anguilla Rostrata Blood Serum; Succinic Acid; Sulfur; Urtica Urens; Viburnum Opulus Root; Wyethia Helenioides Root.

Product ID17089-299_7e029048-a7aa-68a5-e053-2a91aa0af0be
NDC17089-299
Product TypeHuman Otc Drug
Proprietary NameGUNA-ALLERGY-PREV
Generic NameAmbrosia 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 FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2006-05-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameAMBROSIA ARTEMISIIFOLIA; ARUNDO PLINIANA ROOT; ASCLEPIAS CURASSAVICA; BLACK CURRANT; CITRIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; INTERFERON GAMMA-1B; HUMAN INTERLEUKIN 12; MANGANESE GLUCONATE; SODIUM PYRUVATE; SODIUM SULFATE; PARIETARIA OFFICINALIS; PHLEUM PRATENSE; ANGUILLA ROSTRATA BLOOD SERUM; SUCCINIC ACID; SULFUR; URTICA URENS; VIBURNUM OPULUS ROOT; WYETHIA HELENIOIDES ROOT
Active Ingredient Strength18 [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; [hp_X]/30mL; g/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 17089-299-18

1 BOTTLE, DROPPER in 1 BOX (17089-299-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-299-18 [17089029918]

GUNA-ALLERGY-PREV SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21

Drug Details

Active Ingredients

IngredientStrength
AMBROSIA ARTEMISIIFOLIA18 [hp_X]/30mL

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