AllergyEase Southwestern 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; Asarum Canadense Root; Cortisone Acetate; Ageratina Aromatica Root; Euphrasia Stricta; Fraxinus Americana Bark; Galphimia Glauca Flowering Top; Helianthus Annuus Flowering Top; Histamine Dihydrochloride; Juniperus Virginiana Twig; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Plantago Major; Saccharomyces Cerevisiae Rna; Rumex Crispus Root; Schoenocaulon Officinale Seed; Jacobaea Vulgaris.
Product ID | 68703-115_99d49750-ba00-4005-aa1e-11600f1bc6e3 |
NDC | 68703-115 |
Product Type | Human Otc Drug |
Proprietary Name | AllergyEase Southwestern |
Generic Name | Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Asarum Canadense, Cortisone Aceticum, Eupatorium Aromaticum, Euphrasia Officinalis, Fraxinus Americana, Galphimia Glauca, Helianthus Annus, Histaminum Hydrochloricum, Juniperus Virginiana, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Plantago Major, Rna, Rumex Crispus, Sabadilla, Senecio Jacobaea |
Dosage Form | Spray |
Route of Administration | ORAL |
Marketing Start Date | 2013-07-02 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Native Remedies, LLC |
Substance Name | ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ONION; ASARUM CANADENSE ROOT; CORTISONE ACETATE; AGERATINA AROMATICA ROOT; EUPHRASIA STRICTA; FRAXINUS AMERICANA BARK; GALPHIMIA GLAUCA FLOWERING TOP; HELIANTHUS ANNUUS FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; JUNIPERUS VIRGINIANA TWIG; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; PLANTAGO MAJOR; SACCHAROMYCES CEREVISIAE RNA; RUMEX CRISPUS ROOT; SCHOENOCAULON OFFICINALE SEED; JACOBAEA VULGARIS |
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; [hp_X]/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 | 2013-07-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-02 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ADENOSINE CYCLIC PHOSPHATE | 12 [hp_X]/59mL |
SPL SET ID: | 93f7893b-f379-42b5-95f1-6e6a29724491 |
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