NDC 44911-0646 Kidnex IV

Ginkgo Biloba, Alpha-ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malicum Acidum, Pyruvic Acid, Succinicum Acidum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Germanium Sesquioxide, Mercurius Vivus, Nux Vomica, Kidney (suis), Lymph Node (suis), Naphthochinonum, Natrum Oxalaceticum, Phosphorus, Urinary Bladder (suis), Aconiticum Acidum, Cis-

NDC Product Code 44911-0646

NDC CODE: 44911-0646

Proprietary Name: Kidnex IV 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: Ginkgo Biloba, Alpha-ketoglutaricum Acidum, Citricum Acidum, Fumaricum Acidum, Malicum Acidum, Pyruvic Acid, Succinicum Acidum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Germanium Sesquioxide, Mercurius Vivus, Nux Vomica, Kidney (suis), Lymph Node (suis), Naphthochinonum, Natrum Oxalaceticum, Phosphorus, Urinary Bladder (suis), Aconiticum Acidum, Cis- 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

NDC 44911-0646-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Kidnex IV with NDC 44911-0646 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Kidnex IV is ginkgo biloba, alpha-ketoglutaricum acidum, citricum acidum, fumaricum acidum, malicum acidum, pyruvic acid, succinicum acidum, argentum metallicum, aurum metallicum, cuprum metallicum, germanium sesquioxide, mercurius vivus, nux vomica, kidney (suis), lymph node (suis), naphthochinonum, natrum oxalaceticum, phosphorus, urinary bladder (suis), aconiticum acidum, cis-. The product's dosage form is liquid and is administered via oral form.

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.

Kidnex IV 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.


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: Energique, Inc.
Labeler Code: 44911
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: 08-23-2021 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: 12-31-2022 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.

Kidnex IV Product Label Images

Kidnex IV 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:

(in each drop): 2.63% of Aconiticum Acidum, Cis- 30X, Alpha-Ketoglutaricum Acidum 8X, 12X, 30X, Argentum Metallicum 12X, Aurum Metallicum 12X, Citricum Acidum 8X, 12X, 30X, Cuprum Metallicum 12X, Fumaricum Acidum 8X, 12X, 30X, Germanium Sesquioxide 12X, Ginkgo Biloba 6X, Kidney (Suis) 12X, 30X, Lymph Node (Suis) 12X, 30X, Malicum Acidum 8X, 12X, 30X, Mercurius Vivus 12X, Naphthochinonum 12X, 30X, Natrum Oxalaceticum 12X, 30X, Nux Vomica 12X, Phosphorus 12X, 30X, Pyruvic Acid 8X, 12X, 30X, Succinicum Acidum 8X, 12X, 30X, Urinary Bladder (Suis) 12X, 30X.

Indications:

May temporarily relieve symptoms of frequent urination and fluid retention.****Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

May temporarily relieve symptoms of frequent urination and fluid retention.****Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

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 tamper evident seal is broken or missing. Store in a cool, dry place.

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.

Directions:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 20% Ethanol.

Questions:

Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579 800.869.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYKIDNEX IV1 fl. oz. (30 ml)

* Please review the disclaimer below.