AllergyEase Plains is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Wormwood; Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Onion; Ambrosia Artemisiifolia; Caulophyllum Thalictroides Root; Conium Maculatum Flowering Top; Cortisone Acetate; Euphrasia Stricta; Fagopyrum Esculentum; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Potassium Chloride; Melilotus Officinalis Top; Sus Scrofa Nasal Mucosa; Sodium Chloride; Saccharomyces Cerevisiae Rna; Rumex Crispus Root; Schoenocaulon Officinale Seed; Claviceps Purpurea Sclerotium.
Product ID | 68703-112_ba29c138-4083-4c10-a745-c5b0e8f81ee7 |
NDC | 68703-112 |
Product Type | Human Otc Drug |
Proprietary Name | AllergyEase Plains |
Generic Name | Absinthium, Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Ambrosia Artemissfolia, Caulophyllum Thalictroides, Conium Maculatum, Cortisone Aceticum, Euphrasia Officinalis, Fagopyrum Esculentum, Galphimia Glauca, Histaminum Hydrochloricum, Kali Muriaticum, Melilotus Officinalis, Mucosa Nasalis Suis, Natrum Muriaticum, Rna, Rumex Crispus, Sabadilla, Secale Cornutum |
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 | WORMWOOD; ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ONION; AMBROSIA ARTEMISIIFOLIA; CAULOPHYLLUM THALICTROIDES ROOT; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; EUPHRASIA STRICTA; FAGOPYRUM ESCULENTUM; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; MELILOTUS OFFICINALIS TOP; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; RUMEX CRISPUS ROOT; SCHOENOCAULON OFFICINALE SEED; CLAVICEPS PURPUREA SCLEROTIUM |
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 | 2013-07-01 |
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 |
---|---|
WORMWOOD | 12 [hp_X]/59mL |
SPL SET ID: | a7ad4e69-16e4-43c0-ae20-00e0fd7d803f |
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