NDC 17089-418

GUNA-ALLERGY T

Ammonium Carbonate - Apis Mellifera - Arsenic Trioxide - Blatta Orientalis - Cupric Acetate - Drimia Maritima Bulb - Epinephrine - Galphimia Glauca Flowering Top - Histamine Dihydrochloride - Luffa Operculata - Manganese Gluconate - Onion - Schoenocaulon Officinale Seed - Sodium Chloride - Sus Scrofa Adrenal Gland - Sus Scrofa Bronchus - Sus Scrofa Nasal Mucosa -

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

Product ID17089-418_7dc7e4f0-042f-54ef-e053-2991aa0ae7f3
NDC17089-418
Product TypeHuman Otc Drug
Proprietary NameGUNA-ALLERGY T
Generic NameAmmonium Carbonate - Apis Mellifera - Arsenic Trioxide - Blatta Orientalis - Cupric Acetate - Drimia Maritima Bulb - Epinephrine - Galphimia Glauca Flowering Top - Histamine Dihydrochloride - Luffa Operculata - Manganese Gluconate - Onion - Schoenocaulon Officinale Seed - Sodium Chloride - Sus Scrofa Adrenal Gland - Sus Scrofa Bronchus - Sus Scrofa Nasal Mucosa -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2010-05-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameEPINEPHRINE; ONION; AMMONIUM CARBONATE; APIS MELLIFERA; ARSENIC TRIOXIDE; BLATTA ORIENTALIS; SUS SCROFA BRONCHUS; CUPRIC ACETATE; GALPHIMIA GLAUCA FLOWERING TOP; SUS SCROFA ADRENAL GLAND; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; MANGANESE GLUCONATE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SCHOENOCAULON OFFICINALE SEED; DRIMIA MARITIMA BULB
Active Ingredient Strength6 [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; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 17089-418-18

1 BOTTLE, DROPPER in 1 BOX (17089-418-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-418-18 [17089041818]

GUNA-ALLERGY T SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.