AllergyEase Southern is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Onion; Alnus Serrulata Bark; Centaurea Benedicta; Chicory Root; Cortisone Acetate; Mucuna Pruriens Fruit Trichome; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Juglans Cinerea Branch Bark/root Bark; Potassium Chloride; Sus Scrofa Nasal Mucosa; Nasturtium Officinale; Sodium Chloride; Toxicodendron Pubescens Leaf; Saccharomyces Cerevisiae Rna; Schoenocaulon Officinale Seed; Sassafras Albidum Root Bark.
Product ID | 68703-114_fda2dd63-4370-4614-9e1c-68dfd169db92 |
NDC | 68703-114 |
Product Type | Human Otc Drug |
Proprietary Name | AllergyEase Southern |
Generic Name | Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Alnus Serrulata, Carduus Benedictus, Cichorium Intybus, Cortisone Aceticum, Dolichos Pruriens, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Juglans Cinerea, Kali Muriaticum, Mucosa Nasalis Suis, Nasturtium, Natrum Muriaticum, Rhus Tox, Rna, Sabadilla, Sassafras Officinale |
Dosage Form | Spray |
Route of Administration | ORAL |
Marketing Start Date | 2013-07-01 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Native Remedies, LLC |
Substance Name | ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ONION; ALNUS SERRULATA BARK; CENTAUREA BENEDICTA; CHICORY ROOT; CORTISONE ACETATE; MUCUNA PRURIENS FRUIT TRICHOME; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; JUGLANS CINEREA BRANCH BARK/ROOT BARK; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; NASTURTIUM OFFICINALE; SODIUM CHLORIDE; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; SASSAFRAS ALBIDUM ROOT BARK |
Active Ingredient Strength | 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; h/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2013-07-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-01 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ADENOSINE CYCLIC PHOSPHATE | 12 [hp_X]/59mL |
SPL SET ID: | 394c4647-a7c8-4c6a-9619-de55754b3aa9 |
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