63083-1021 NDC - NORTHEAST REGIONAL

Drug Information

Product NDC: 63083-1021

Proprietary Name: Northeast Regional

Non Proprietary Name: Northeast Regional

Active Ingredient(s):
  • 6 [hp_X]/59mL ACER NEGUNDO ROOT BARK;
  • 6 [hp_X]/59mL AMARANTHUS HYBRIDUS LEAF;
  • 6 [hp_X]/59mL AMBROSIA ARTEMISIIFOLIA WHOLE;
  • 6 [hp_X]/59mL BASSIA SCOPARIA FRUIT;
  • 6 [hp_X]/59mL BEEF LIVER;
  • 6 [hp_X]/59mL BETULA OCCIDENTALIS POLLEN;
  • 6 [hp_X]/59mL CARYA LACINIOSA BARK;
  • 6 [hp_X]/59mL CHENOPODIUM ALBUM POLLEN;
  • 6 [hp_X]/59mL CORTICOTROPIN;
  • 6 [hp_X]/59mL CYNODON DACTYLON WHOLE;
  • 6 [hp_X]/59mL ELM;
  • 6 [hp_X]/59mL ENGLISH WALNUT;
  • 6 [hp_X]/59mL FRAXINUS LATIFOLIA WHOLE;
  • 12 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE;
  • 6 [hp_X]/59mL IVA ANGUSTIFOLIA WHOLE;
  • 6 [hp_X]/59mL LIGUSTRUM LUCIDUM SEED;
  • 6 [hp_X]/59mL MEDICAGO SATIVA WHOLE;
  • 6 [hp_X]/59mL MILLETTIA PINNATA WHOLE;
  • 6 [hp_X]/59mL NEUROTENSIN;
  • 6 [hp_X]/59mL PINUS PONDEROSA POLLEN;
  • 6 [hp_X]/59mL PLANTAGO LANCEOLATA LEAF;
  • 6 [hp_X]/59mL POPULUS FREMONTII POLLEN;
  • 6 [hp_X]/59mL POPULUS TREMULOIDES POLLEN;
  • 6 [hp_X]/59mL QUERCUS KELLOGGII POLLEN;
  • 6 [hp_X]/59mL RUMEX CRISPUS ROOT;
  • 6 [hp_X]/59mL SAGE;
  • 6 [hp_X]/59mL SUAEDA MARITIMA FLOWERING TOP;
  • 6 [hp_X]/59mL SUS SCROFA ADRENAL GLAND;
  • 6 [hp_X]/59mL SYMPHORICARPOS ALBUS FRUIT;
  • 6 [hp_X]/59mL WHITE MULBERRY;
  • 6 [hp_X]/59mL XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Adrenocorticotropic Hormone [CS];
  • Adrenocorticotropic Hormone [EPC];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Meat Proteins [EXT];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Nut Proteins [EXT];
  • Plant Proteins [CS];
  • Pollen [CS];
  • Pollen [CS];
  • Pollen [CS];
  • Pollen [CS];
  • Pollen [CS];
  • Pollen [CS];
  • Pollen [CS];
  • Pollen [CS]

Labeler Information

Labeler Name: Professional Complementary Health Formulas
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/15/1984

Package Information

No. Package Code Package Description Billing Unit
163083-1021-259 mL in 1 BOTTLE, DROPPER (63083-1021-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63083-1021The 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 NAMENortheast RegionalThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX1021A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMENortheast RegionalThe 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 DATE8/15/1984This 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 NAMEProfessional Complementary Health FormulasName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACER NEGUNDO ROOT BARK; AMARANTHUS HYBRIDUS LEAF; AMBROSIA ARTEMISIIFOLIA WHOLE; BASSIA SCOPARIA FRUIT; BEEF LIVER; BETULA OCCIDENTALIS POLLEN; CARYA LACINIOSA BARK; CHENOPODIUM ALBUM POLLEN; CORTICOTROPIN; CYNODON DACTYLON WHOLE; ELM; ENGLISH WALNUT; FRAXINUS LATIFOLIA WHOLE; HISTAMINE DIHYDROCHLORIDE; IVA ANGUSTIFOLIA WHOLE; LIGUSTRUM LUCIDUM SEED; MEDICAGO SATIVA WHOLE; MILLETTIA PINNATA WHOLE; NEUROTENSIN; PINUS PONDEROSA POLLEN; PLANTAGO LANCEOLATA LEAF; POPULUS FREMONTII POLLEN; POPULUS TREMULOIDES POLLEN; QUERCUS KELLOGGII POLLEN; RUMEX CRISPUS ROOT; SAGE; SUAEDA MARITIMA FLOWERING TOP; SUS SCROFA ADRENAL GLAND; SYMPHORICARPOS ALBUS FRUIT; WHITE MULBERRY; XANTHIUM STRUMARIUM VAR. CANADENSE POLLENAn 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 STRENGTH6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 12; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6 
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; [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 CLASSESAdrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Meat Proteins [EXT], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Nut Proteins [EXT], Plant Proteins [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS], Pollen [CS] 

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