NDC 50181-0010 Mbm 3 Heart-shock

Phytolacca Decandra, Spongia Tosta, Crocus Sativus, Coffea Cruda, Aurum Metallicum

NDC Product Code 50181-0010

NDC CODE: 50181-0010

Proprietary Name: Mbm 3 Heart-shock 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: Phytolacca Decandra, Spongia Tosta, Crocus Sativus, Coffea Cruda, Aurum Metallicum 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

  • 50181 - The Wellness Center For Research And Education

NDC 50181-0010-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Mbm 3 Heart-shock with NDC 50181-0010 is a a human over the counter drug product labeled by The Wellness Center For Research And Education. The generic name of Mbm 3 Heart-shock is phytolacca decandra, spongia tosta, crocus sativus, coffea cruda, aurum metallicum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: The Wellness Center For Research And Education

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.

Mbm 3 Heart-shock 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.

  • PHYTOLACCA AMERICANA ROOT 3 [hp_C]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_C]/mL
  • SAFFRON 34 [hp_C]/mL
  • ARABICA COFFEE BEAN 34 [hp_C]/mL
  • GOLD 34 [hp_C]/mL

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.

  • WATER (UNII: 059QF0KO0R)
  • 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: The Wellness Center For Research And Education
Labeler Code: 50181
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: 10-24-2012 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: 12-31-2021 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 - NO 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".

* Please review the disclaimer below.

Mbm 3 Heart-shock Product Label Images

Mbm 3 Heart-shock 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:

Phytolacca Decandra 3C, Spongia Tosta 3C, Crocus Sativus 34C, Coffea Cruda 34C, 89C, Aurum Metallicum 34C, 89C, 144C.

Indications:

For temporary relief of shock, excessive joy, guilt, and feelings of being overwhelmed.

For temporary relief of shock, excessive joy, guilt, and feelings of being overwhelmed.

Warnings:

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if seal is broken or missing.

Directions:

Feel the emotion fully, breathe deeply-connected breaths. Put 5 drops under tongue to release emotion. Continue 5 drops 2 times daily as needed. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol.

Keep Out Of Reach Of Children:

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Questions:

MFD FOR:The Wellness Center for Researchand Education, Inc.1237 S. Victoria Ave. Suite 169Oxnard, CA 93035

Package Label Display:

Dr. Theresa Dale'sMIND BODY MERIDIANNDC: 50181-0010-1Fibonacci SeriesMBM 3Heart-ShockShock, Trauma,OverwhelmHOMEOPATHIC1 fluid oz. (30 ml)

* Please review the disclaimer below.