73421-2208 NDC - WHOLE SYSTEM EEP (BELLADONNA, BERBER VULG, CAUSTICUM, CEANOTHUS, CHELIDONIUM MAJ, CINCHONA, COFFEA CRUDA, CONDURANGO, GRAPHITES, HYDRASTIS, IGNATIA, LILIUM, LYCOPODIUM, , MERC CORROS, NUX VOM, PANCREAS, SCROPHULARIA NODOSA, SENNA, SPONGIA, ZINC MET)

Drug Information

  • Product NDC: 73421-2208
  • Proprietary Name: Whole System Eep
  • Non Proprietary Name: Belladonna, Berber vulg, Causticum, Ceanothus, Chelidonium maj, Cinchona, Coffea cruda, Condurango, Graphites, Hydrastis, Ignatia, Lilium, Lycopodium, , Merc corros, Nux vom, Pancreas, Scrophularia nodosa, Senna, Spongia, Zinc met
  • Active Ingredient(s): 1 [hp_M]/29.6mL ARABICA COFFEE BEAN; 1 [hp_M]/29.6mL ATROPA BELLADONNA; 12 [hp_X]/29.6mL BERBERIS VULGARIS ROOT BARK; 1 [hp_M]/29.6mL CAUSTICUM; 6 [hp_X]/29.6mL CEANOTHUS AMERICANUS LEAF; 3 [hp_X]/29.6mL CHELIDONIUM MAJUS WHOLE; 1 [hp_M]/29.6mL CINCHONA BARK; 5 [hp_X]/29.6mL GOLDENSEAL; 1 [hp_M]/29.6mL GRAPHITE; 1 [hp_M]/29.6mL LILIUM LANCIFOLIUM WHOLE FLOWERING; 12 [hp_X]/29.6mL LYCOPODIUM CLAVATUM SPORE; 3 [hp_X]/29.6mL MARSDENIA CONDURANGO BARK; 12 [hp_X]/29.6mL MERCURIC CHLORIDE; 15 [hp_X]/29.6mL SCROPHULARIA NODOSA WHOLE; 3 [hp_X]/29.6mL SENNA LEAF; 6 [hp_X]/29.6mL SPONGIA OFFICINALIS SKELETON, ROASTED; 200 [hp_X]/29.6mL STRYCHNOS IGNATII SEED; 1 [hp_M]/29.6mL STRYCHNOS NUX-VOMICA SEED; 12 [hp_X]/29.6mL SUS SCROFA PANCREAS; 1 [hp_M]/29.6mL ZINC
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: White Manufacturing Inc. DBA Micro-West
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/1/2021

Package Information

No. Package Code Package Description Billing Unit
173421-2208-129.6 mL in 1 BOTTLE (73421-2208-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73421-2208The 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 NAMEWhole System EepThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBelladonna, Berber vulg, Causticum, Ceanothus, Chelidonium maj, Cinchona, Coffea cruda, Condurango, Graphites, Hydrastis, Ignatia, Lilium, Lycopodium, , Merc corros, Nux vom, Pancreas, Scrophularia nodosa, Senna, Spongia, Zinc metThe 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 DATE6/1/2021This 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 NAMEWhite Manufacturing Inc. DBA Micro-WestName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARABICA COFFEE BEAN; ATROPA BELLADONNA; BERBERIS VULGARIS ROOT BARK; CAUSTICUM; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS WHOLE; CINCHONA BARK; GOLDENSEAL; GRAPHITE; LILIUM LANCIFOLIUM WHOLE FLOWERING; LYCOPODIUM CLAVATUM SPORE; MARSDENIA CONDURANGO BARK; MERCURIC CHLORIDE; SCROPHULARIA NODOSA WHOLE; SENNA LEAF; SPONGIA OFFICINALIS SKELETON, ROASTED; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA PANCREAS; ZINCAn 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 STRENGTH1; 1; 12; 1; 6; 3; 1; 5; 1; 1; 12; 3; 12; 15; 3; 6; 200; 1; 12; 1 
ACTIVE INGRED UNIT[hp_M]/29.6mL; [hp_M]/29.6mL; [hp_X]/29.6mL; [hp_M]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_M]/29.6mL; [hp_X]/29.6mL; [hp_M]/29.6mL; [hp_M]/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_M]/29.6mL; [hp_X]/29.6mL; [hp_M]/29.6mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Seed Storage Proteins [CS] 

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This page was last updated on: 11/21/2025

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