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NDC 61657-0208 Whole System Eep

Mercurius Corrosivus, Nux Vomica, Hyoscyaminum, Carcinosinum, Graphites, Zincum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61657-0208?
  4. Whole System Eep Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
61657-0208
Proprietary Name:
Whole System Eep
Non-Proprietary Name: [1]
Mercurius Corrosivus, Nux Vomica, Hyoscyaminum, Carcinosinum, Graphites, Zincum Metallicum, Lilium Tigrinum, Cinchona Officinalis, Causticum, Coffea Cruda, Belladonna, Ignatia Amara, Scrophularia Nodosa, Spongia Tosta , Ceanothus Americanus, Senna, Hydrastis Canadensis, Condurango, Chelidonium Majus, Pituitary Gland, Bos Taurus, Pancreas Suis, Lycopodium Clavatum, Berberis Vulgaris,
Substance Name: [2]
Arabica Coffee Bean; Atropa Belladonna; Berberis Vulgaris Root Bark; Bos Taurus Pituitary Gland; Causticum; Ceanothus Americanus Leaf; Chelidonium Majus; Cinchona Officinalis Bark; Goldenseal; Graphite; Human Breast Tumor Cell; Hyoscyamine; Lilium Lancifolium Whole Flowering; Lycopodium Clavatum Spore; Marsdenia Condurango Bark; Mercuric Chloride; Scrophularia Nodosa; Senna Leaf; Spongia Officinalis Skeleton, Roasted; Strychnos Ignatii Seed; Strychnos Nux-vomica Seed; Sus Scrofa Pancreas; Zinc
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    White Manufacturing Inc. Dba Micro-west
    Labeler Code:
    61657
    Product Label ID:
    6fe11fe3-6725-4701-8461-25d4e885a6c4
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-21-2005
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 61657-0208?

    The NDC code 61657-0208 is assigned by the FDA to the product Whole System Eep which is a human over the counter drug product labeled by White Manufacturing Inc. Dba Micro-west. The generic name of Whole System Eep is mercurius corrosivus, nux vomica, hyoscyaminum, carcinosinum, graphites, zincum metallicum, lilium tigrinum, cinchona officinalis, causticum, coffea cruda, belladonna, ignatia amara, scrophularia nodosa, spongia tosta , ceanothus americanus, senna, hydrastis canadensis, condurango, chelidonium majus, pituitary gland, bos taurus, pancreas suis, lycopodium clavatum, berberis vulgaris, . The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 61657-0208-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Whole System Eep?

    INDICATIONS: For the temporary relief of depresson, energy loss, anxiety

    What are Whole System Eep Active Ingredients?

    An 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.

    Which are Whole System Eep UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Whole System Eep Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Whole System Eep?

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An 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.

    [3] What kind of product is this? - Indicates 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".