NDC 61657-0208 Whole System Eep

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,

NDC Product Code 61657-0208

NDC Code: 61657-0208

Proprietary Name: Whole System Eep What is the Proprietary Name?
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 Name: 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, 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.

NDC Code Structure

  • 61657 - White Manufacturing Inc. Dba Micro-west
    • 61657-0208 - Whole System Eep

NDC 61657-0208-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Whole System Eep with NDC 61657-0208 is a 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.

Labeler Name: White Manufacturing Inc. Dba Micro-west

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.

Product Type: Human Otc Drug 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.

Whole System Eep Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • MERCURIC CHLORIDE 12 [hp_X]/30mL
  • BERBERIS VULGARIS ROOT BARK 12 [hp_X]/30mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/30mL
  • SUS SCROFA PANCREAS 12 [hp_X]/30mL
  • BOS TAURUS PITUITARY GLAND 12 [hp_X]/30mL
  • CHELIDONIUM MAJUS 3 [hp_X]/30mL
  • MARSDENIA CONDURANGO BARK 3 [hp_X]/30mL
  • GOLDENSEAL 3 [hp_X]/30mL
  • SENNA LEAF 3 [hp_X]/30mL
  • CEANOTHUS AMERICANUS LEAF 6 [hp_X]/30mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_X]/30mL
  • SCROPHULARIA NODOSA 15 [hp_X]/30mL
  • STRYCHNOS IGNATII SEED 200 [hp_X]/30mL
  • ATROPA BELLADONNA 1 [hp_M]/30mL
  • ARABICA COFFEE BEAN 1 [hp_M]/30mL
  • CAUSTICUM 5 [hp_M]/30mL
  • CINCHONA OFFICINALIS BARK 5 [hp_M]/30mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 5 [hp_M]/30mL
  • ZINC 3 [hp_M]/30mL
  • GRAPHITE 2 [hp_M]/30mL
  • HUMAN BREAST TUMOR CELL 10 [hp_M]/30mL
  • HYOSCYAMINE 10 [hp_M]/30mL
  • STRYCHNOS NUX-VOMICA SEED 10 [hp_M]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: White Manufacturing Inc. Dba Micro-west
Labeler Code: 61657
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 05-21-2005 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Whole System Eep Product Label Images

Whole System Eep Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Belladonna 1MBerber vulg 12XCausticum 5MCeanothus 6XChelidonium maj 3XCinchona 5MCoffea cruda 1MCondurango 3XGraphites 2MHydrastis 3XHysocyaminum 10MIgnatia 200xLillium 5MLycopodium 12XMerc corros 12XNux vom 10MPancreas suis 12XScrophularia nodosa 15XSenna 3XSpongia 6XZinc met 3M

Purpose

For the temporary relief of depresson, energy loss, anxiety

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Warnings Section

WARNINGS: WARNINGS: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediatelyOTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact

Indications

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

Inactive Ingredients

Alcohol 20% v/vPurified water

Directions

DIRECTIONS: Take 6 drops orally, 4 times a day. For ages 2 to adult

Manufacture

MANUFACTURED FOR MICRO-WESTP.O. BOX 950DOUGLAS, WY 826331-307-358-5066

* Please review the disclaimer below.

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