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NDC 64578-0178 Dental-chord

Aceticum Acidum,Ammonium Muriaticum,Argentum Metallicum,Aurum Metallicum,Calcarea - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64578-0178?
  4. Active Ingredients
  5. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 64578-0178 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
64578-0178
Proprietary Name:
Dental-chord
Non-Proprietary Name: [1]
Aceticum Acidum, Ammonium Muriaticum, Argentum Metallicum, Aurum Metallicum, Calcarea Fluorica, Calcarea Phosphorica, Carbolicum Acidum, Citrus Limonum, Cuprum Metallicum, Ferrum Metallicum, Glycyrrhiza Glabra, Lappa Major, Medulla Ossis Suis, Mercurius Solubilis, Myrrha, Natrum Fluoratum, Palladium Metallicum, Phosphoricum Acidum, Phytolacca Decandra, Selenium Metallicum, Silicea, Stannum Metallicum, Staphysagria, Stillingia Sylvatica, Trifolium Pratense, X-ray, Zincum Oxydatum
Substance Name: [2]
Acetic Acid; Ammonium Chloride; Arctium Lappa Root; Calcium Fluoride; Copper; Delphinium Staphisagria Seed; Glycyrrhiza Glabra; Gold; Iron; Lactose, X-ray Exposed (1000 Rad); Lemon Juice; Mercurius Solubilis; Myrrh; Palladium; Phenol; Phosphoric Acid; Phytolacca Americana Root; Selenium; Silicon Dioxide; Silver; Sodium Fluoride; Stillingia Sylvatica Root; Sus Scrofa Bone Marrow; Tin; Tribasic Calcium Phosphate; Trifolium Pratense Flower; Zinc Oxide
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]
Energetix Corporation
Labeler Code:
64578
Product Label ID:
6c9ba926-7c35-49fd-94d8-988ca0bb772c
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
09-04-2014
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 64578-0178?

The NDC code 64578-0178 is assigned by the FDA to the product Dental-chord which is a human over the counter drug product labeled by Energetix Corporation. The generic name of Dental-chord is aceticum acidum, ammonium muriaticum, argentum metallicum, aurum metallicum, calcarea fluorica, calcarea phosphorica, carbolicum acidum, citrus limonum, cuprum metallicum, ferrum metallicum, glycyrrhiza glabra, lappa major, medulla ossis suis, mercurius solubilis, myrrha, natrum fluoratum, palladium metallicum, phosphoricum acidum, phytolacca decandra, selenium metallicum, silicea, stannum metallicum, staphysagria, stillingia sylvatica, trifolium pratense, x-ray, zincum oxydatum. 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 64578-0178-1 59.1 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 Dental-chord 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 the Pharmacologic Classes for Dental-chord?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".