NDC 17089-461

GUNA ALLERGY

Adrenalinum - Allium Cepa - Ammonium Carbonicum - Apis Mellifica - Argentum Nitricum - Arsenicum Album - Cuprum Aceticum - Galphimia Glauca - Glandula Suprarenalis Suis - Histaminum Hydrochloricum - Luffa Operculata - Matricaria Chamomilla - Mucosa Nasalis Suis - Natrum Muriaticum - Sabadilla - Scilla Maritima -

GUNA ALLERGY is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Histamine Dihydrochloride; Sus Scrofa Adrenal Gland; Epinephrine; Apis Mellifera; Cupric Acetate; Silver Nitrate; Drimia Maritima Bulb; Galphimia Glauca Flowering Top; Schoenocaulon Officinale Seed; Sodium Chloride; Luffa Operculata Fruit; Matricaria Chamomilla Whole; Ammonium Carbonate; Onion; Arsenic Trioxide; Sus Scrofa Nasal Mucosa.

Product ID17089-461_ae6bd5dc-eb2c-1d87-e053-2a95a90a97d9
NDC17089-461
Product TypeHuman Otc Drug
Proprietary NameGUNA ALLERGY
Generic NameAdrenalinum - Allium Cepa - Ammonium Carbonicum - Apis Mellifica - Argentum Nitricum - Arsenicum Album - Cuprum Aceticum - Galphimia Glauca - Glandula Suprarenalis Suis - Histaminum Hydrochloricum - Luffa Operculata - Matricaria Chamomilla - Mucosa Nasalis Suis - Natrum Muriaticum - Sabadilla - Scilla Maritima -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2020-09-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameHISTAMINE DIHYDROCHLORIDE; SUS SCROFA ADRENAL GLAND; EPINEPHRINE; APIS MELLIFERA; CUPRIC ACETATE; SILVER NITRATE; DRIMIA MARITIMA BULB; GALPHIMIA GLAUCA FLOWERING TOP; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; LUFFA OPERCULATA FRUIT; MATRICARIA CHAMOMILLA WHOLE; AMMONIUM CARBONATE; ONION; ARSENIC TRIOXIDE; SUS SCROFA NASAL MUCOSA
Active Ingredient Strength200 [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; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 17089-461-18

1 BOTTLE, DROPPER in 1 BOX (17089-461-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2020-09-24
NDC Exclude FlagN
Sample Package?N

Drug Details


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