Allergies Northeastern US is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by New Sun Inc.. The primary component is Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Hyacinthoides Non-scripta; Onion; Collinsonia Canadensis Root; Cortisone Acetate; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Saccharomyces Cerevisiae Rna; Rumex Crispus Root; Schoenocaulon Officinale Seed; Sage; Tanacetum Vulgare Top; Trifolium Pratense Flower; Vinca Minor.
Product ID | 66579-0037_3fd0b083-1d2b-4d50-bd50-c431b4567599 |
NDC | 66579-0037 |
Product Type | Human Otc Drug |
Proprietary Name | Allergies Northeastern US |
Generic Name | Adenosinum Cyclophosphoricum, Adren Alinum, Adrenocorticotrophin, Agraphis Nutans, Allium Cepa, Collinsonia Canadensis, Cortisone Aceticum, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Rna, Rumex Crispus, Sabadilla, Salvia Officinalis, Tanacetum Vulgare, Trifolium Pratense, Vinca Minor |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2012-04-17 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | New Sun Inc. |
Substance Name | ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; HYACINTHOIDES NON-SCRIPTA; ONION; COLLINSONIA CANADENSIS ROOT; CORTISONE ACETATE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; RUMEX CRISPUS ROOT; SCHOENOCAULON OFFICINALE SEED; SAGE; TANACETUM VULGARE TOP; TRIFOLIUM PRATENSE FLOWER; VINCA MINOR |
Active Ingredient Strength | 12 [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL; [hp_X]/29mL |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2012-04-17 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-04-17 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ADENOSINE CYCLIC PHOSPHATE | 12 [hp_X]/29mL |
SPL SET ID: | 1b332a21-6ebc-4462-8fc9-8645159d1c87 |
Manufacturer | |
UNII |