NDC 57955-8315

Midwest Regional Allergies

Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Ambrosia Artemisiaefolia, Cichorium Intybus, Conium Maculatum, Cortisone Aceticum, Euphrasia Officinalis, Fagopyrum Esculentum, Galphimia Glauca, Hedera Helix, Histaminum Hydrochloricum, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Rna, Rumex Crispus, Sabadilla, Secale Cornutum

Midwest Regional Allergies is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Onion; Ambrosia Artemisiifolia; Chicory Root; Conium Maculatum Flowering Top; Cortisone Acetate; Euphrasia Stricta; Fagopyrum Esculentum; Galphimia Glauca Flowering Top; Hedera Helix Flowering Twig; Histamine Dihydrochloride; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Saccharomyces Cerevisiae Rna; Rumex Crispus Root; Schoenocaulon Officinale Seed; Claviceps Purpurea Sclerotium.

Product ID57955-8315_0d634610-703e-48c5-9356-8bdefe43ebd7
NDC57955-8315
Product TypeHuman Otc Drug
Proprietary NameMidwest Regional Allergies
Generic NameAdenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Ambrosia Artemisiaefolia, Cichorium Intybus, Conium Maculatum, Cortisone Aceticum, Euphrasia Officinalis, Fagopyrum Esculentum, Galphimia Glauca, Hedera Helix, Histaminum Hydrochloricum, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Rna, Rumex Crispus, Sabadilla, Secale Cornutum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-11-04
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKing Bio Inc.
Substance NameADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ONION; AMBROSIA ARTEMISIIFOLIA; CHICORY ROOT; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; EUPHRASIA STRICTA; FAGOPYRUM ESCULENTUM; GALPHIMIA GLAUCA FLOWERING TOP; HEDERA HELIX FLOWERING TWIG; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; RUMEX CRISPUS ROOT; SCHOENOCAULON OFFICINALE SEED; CLAVICEPS PURPUREA SCLEROTIUM
Active Ingredient Strength10 [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 57955-8315-1

1 BOTTLE, SPRAY in 1 CARTON (57955-8315-1) > 29.6 mL in 1 BOTTLE, SPRAY
Marketing Start Date2013-11-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57955-8315-1 [57955831501]

Midwest Regional Allergies LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-11-04
Inactivation Date2020-01-31

Drug Details


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