57955-2807 NDC - REGIONAL ALLERGIES GREAT LAKES U.S. (ADENOSINUM CYCLOPHOSPHORICUM, ADRENALINUM, ADRENOCORTICOTROPHIN, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARUM TRIPHYLLUM, ARUNDO MAURITANICA, CHELIDONIUM MAJUS, CHENOPODIUM VULVARIA, CICHORIUM INTYBUS, CORTISONE ACETICUM, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HEDERA HELIX, HISTAMINUM HYDROCHLORICUM, JUGLANS CINEREA, KALI MURIATICUM, NATRUM MURIATICUM, PULSATILLA, RNA, SABADILLA, TEUCRIUM SCORODONIA.)

Drug Information

Product NDC: 57955-2807

Proprietary Name: Regional Allergies Great Lakes U.S.

Non Proprietary Name: Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium cepa, Ambrosia artemisiaefolia, Arum triphyllum, Arundo mauritanica, Chelidonium majus, Chenopodium vulvaria, Cichorium intybus, Cortisone aceticum, Euphrasia officinalis, Galphimia glauca, Hedera helix, Histaminum hydrochloricum, Juglans cinerea, Kali muriaticum, Natrum muriaticum, Pulsatilla, RNA, Sabadilla, Teucrium scorodonia.

Active Ingredient(s):
  • 12 [hp_X]/59mL ADENOSINE CYCLIC PHOSPHATE;
  • 12 [hp_X]/59mL AMBROSIA ARTEMISIIFOLIA WHOLE;
  • 12 [hp_X]/59mL ARISAEMA TRIPHYLLUM ROOT;
  • 12 [hp_X]/59mL ARUNDO PLINIANA ROOT;
  • 112 [hp_X]/59mL CHELIDONIUM MAJUS WHOLE;
  • 12 [hp_X]/59mL CHENOPODIUM VULVARIA WHOLE;
  • 12 [hp_X]/59mL CHICORY ROOT;
  • 30 [hp_X]/59mL CORTICOTROPIN;
  • 12 [hp_X]/59mL CORTISONE ACETATE;
  • 12 [hp_X]/59mL EPINEPHRINE;
  • 12 [hp_X]/59mL EUPHRASIA STRICTA;
  • 12 [hp_X]/59mL GALPHIMIA GLAUCA FLOWERING TOP;
  • 12 [hp_X]/59mL HEDERA HELIX FLOWERING TWIG;
  • 12 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE;
  • 12 [hp_X]/59mL JUGLANS CINEREA BRANCH BARK/ROOT BARK;
  • 30 [hp_X]/59mL ONION;
  • 12 [hp_X]/59mL POTASSIUM CHLORIDE;
  • 12 [hp_X]/59mL PULSATILLA VULGARIS WHOLE;
  • 12 [hp_X]/59mL SACCHAROMYCES CEREVISIAE RNA;
  • 12 [hp_X]/59mL SCHOENOCAULON OFFICINALE SEED;
  • 12 [hp_X]/59mL SODIUM CHLORIDE;
  • 12 [hp_X]/59mL TEUCRIUM SCORODONIA FLOWERING TOP


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Adrenergic alpha-Agonists [MoA];
  • Adrenergic beta-Agonists [MoA];
  • Adrenocorticotropic Hormone [CS];
  • Adrenocorticotropic Hormone [EPC];
  • Allergens [CS];
  • Catecholamine [EPC];
  • Catecholamines [CS];
  • Cell-mediated Immunity [PE];
  • Corticosteroid Hormone Receptor Agonists [MoA];
  • Corticosteroid [EPC];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC];
  • Vegetable Proteins [CS];
  • alpha-Adrenergic Agonist [EPC];
  • beta-Adrenergic Agonist [EPC]

Labeler Information

Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/14/2022

Package Information

No. Package Code Package Description Billing Unit
157955-2807-21 BOTTLE, SPRAY in 1 CARTON (57955-2807-2) / 59 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-2807The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMERegional Allergies Great Lakes U.S.The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium cepa, Ambrosia artemisiaefolia, Arum triphyllum, Arundo mauritanica, Chelidonium majus, Chenopodium vulvaria, Cichorium intybus, Cortisone aceticum, Euphrasia officinalis, Galphimia glauca, Hedera helix, Histaminum hydrochloricum, Juglans cinerea, Kali muriaticum, Natrum muriaticum, Pulsatilla, RNA, Sabadilla, Teucrium scorodonia.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/14/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEKing Bio Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE CYCLIC PHOSPHATE; AMBROSIA ARTEMISIIFOLIA WHOLE; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; CHELIDONIUM MAJUS WHOLE; CHENOPODIUM VULVARIA WHOLE; CHICORY ROOT; CORTICOTROPIN; CORTISONE ACETATE; EPINEPHRINE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HEDERA HELIX FLOWERING TWIG; HISTAMINE DIHYDROCHLORIDE; JUGLANS CINEREA BRANCH BARK/ROOT BARK; ONION; POTASSIUM CHLORIDE; PULSATILLA VULGARIS WHOLE; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; TEUCRIUM SCORODONIA FLOWERING TOPAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 112; 12; 12; 30; 12; 12; 12; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[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; [hp_X]/59mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 2/1/2023