AllergyEase Great Lakes is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Silver Star Brands, Inc. The primary component is Chelidonium Majus; Chenopodium Vulvaria; Chicory Root; Cortisone Acetate; Euphrasia Stricta; Galphimia Glauca Flowering Top; Hedera Helix Flowering Twig; Histamine Dihydrochloride; Juglans Cinerea Branch Bark/root Bark; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Anemone Patens; Saccharomyces Cerevisiae Rna; Schoenocaulon Officinale Seed; Teucrium Scorodonia Flowering Top; Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Onion; Ambrosia Artemisiifolia.
| Product ID | 68703-109_1b00a71e-2207-7392-e054-00144ff88e88 |
| NDC | 68703-109 |
| Product Type | Human Otc Drug |
| Proprietary Name | AllergyEase Great Lakes |
| Generic Name | Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Ambrosia Artemisiaefolia, Chelidonium Majus, Chenopodium Vulvaria, Cichorium Intybus, Cortisone Aceticum, Euphrasia Officinalis, Galphimia Glauca, Hereda Helix, Histaminum Hydrochloricum, Junglans Cinerea, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Pulsatilla Nuttalliana, Rna, Sabadilla, Teucrium Scorodonia |
| Dosage Form | Spray |
| Route of Administration | ORAL |
| Marketing Start Date | 2013-06-28 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Silver Star Brands, Inc |
| Substance Name | CHELIDONIUM MAJUS; CHENOPODIUM VULVARIA; CHICORY ROOT; CORTISONE ACETATE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HEDERA HELIX FLOWERING TWIG; HISTAMINE DIHYDROCHLORIDE; JUGLANS CINEREA BRANCH BARK/ROOT BARK; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; ANEMONE PATENS; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; TEUCRIUM SCORODONIA FLOWERING TOP; ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ONION; AMBROSIA ARTEMISIIFOLIA |
| 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 | 2013-06-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-06-28 |
| Marketing End Date | 2020-02-11 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-11 |
| Ingredient | Strength |
|---|---|
| CHELIDONIUM MAJUS | 12 [hp_X]/59mL |
| SPL SET ID: | b656126c-13db-4013-9a86-4c037a03d6d3 |
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