NDC 50181-0012 4 Kidney

Solidago Virgaurea, Berberis Vulgaris, Aconitum Napellus, Argentum Nitricum, Arnica Montana, Nitricum Acidum

NDC Product Code 50181-0012

NDC CODE: 50181-0012

Proprietary Name: 4 Kidney 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: Solidago Virgaurea, Berberis Vulgaris, Aconitum Napellus, Argentum Nitricum, Arnica Montana, Nitricum Acidum 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

NDC 50181-0012-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

4 Kidney with NDC 50181-0012 is a a human over the counter drug product labeled by The Wellness Center. The generic name of 4 Kidney is solidago virgaurea, berberis vulgaris, aconitum napellus, argentum nitricum, arnica montana, nitricum acidum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: The Wellness Center

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.

4 Kidney 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.

  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 30 [hp_C]/mL
  • ACONITUM NAPELLUS 1 [hp_M]/mL
  • ARNICA MONTANA 1 [hp_M]/mL
  • SILVER NITRATE 1 [hp_M]/mL
  • NITRIC ACID 1 [hp_M]/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
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: 10-12-2012 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".

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4 Kidney Product Label Images

4 Kidney 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

Solidago Virgaurea 3X, 30C, Berberis Vulgaris 30C, Aconitum Napellus 1M, Argentum Nitricum 1M, Arnica Montana 1M, Nitricum Acidum 1M.

Indications

For temporary relief of fear.

Warnings

If pregnant or breastfeeding, 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 tamper evident seal is brokenor missing. Store in a cool, dry place.

Directions

Feel the emotion fully, breathe deeply-connecting breaths. Put 5 drops under tongue to release emotion. Continue 5 drops 2x 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

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

Indications And Usage

For temporary relief of fear.

Questions

MFD FOR:The Wellness Center for Researchand Education, Inc.1237 S. Victoria Ave., Suite 169Oxnard, CA 930351-866-962-6484

Package Label Display

Dr. Theresa Dale'sNDC: 50181-0012-1HomeopathicNeuro-Emotional Remedies4 KIDNEYFear 1 fl oz (30 ml)

* Please review the disclaimer below.