NDC 66579-0037

Allergies Northeastern US

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

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 ID66579-0037_3fd0b083-1d2b-4d50-bd50-c431b4567599
NDC66579-0037
Product TypeHuman Otc Drug
Proprietary NameAllergies Northeastern US
Generic NameAdenosinum 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 FormLiquid
Route of AdministrationORAL
Marketing Start Date2012-04-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNew Sun Inc.
Substance NameADENOSINE 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 Strength12 [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 FlagE
Listing Certified Through2018-12-31

Packaging

NDC 66579-0037-1

29 mL in 1 BOTTLE, SPRAY (66579-0037-1)
Marketing Start Date2012-04-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66579-0037-1 [66579003701]

Allergies Northeastern US LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-17
Inactivation Date2020-01-31

Drug Details


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