NDC 44911-0668 Psora Miasm
Eggshell Membrane, Whey Protein, Calcarea Carbonica, Lycopodium Clavatum, Sulphur, Ar...

Product Information

What is NDC 44911-0668?

The NDC code 44911-0668 is assigned by the FDA to the product Psora Miasm which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Psora Miasm is eggshell membrane, whey protein, calcarea carbonica, lycopodium clavatum, sulphur, arsenicum album, fagopyrum esculentum, graphites, hydrocotyle asiatica, natrum muriaticum. 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 44911-0668-1 30 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, RxNorm crosswalk and the complete product label.

NDC Product Code	44911-0668
Proprietary Name 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.	Psora Miasm
Non-Proprietary Name 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.	Eggshell Membrane, Whey Protein, Calcarea Carbonica, Lycopodium Clavatum, Sulphur, Arsenicum Album, Fagopyrum Esculentum, Graphites, Hydrocotyle Asiatica, Natrum Muriaticum
Substance Name 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.	Arsenic Trioxide; Centella Asiatica Whole; Egg Shell Membrane; Fagopyrum Esculentum Whole; Graphite; Lycopodium Clavatum Spore; Oyster Shell Calcium Carbonate, Crude; Sodium Chloride; Sulfur; Whey
Product Type 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.	Human Otc Drug
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) 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.	Energique, Inc.
Labeler Code	44911
Marketing Category 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.	UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.	03-15-2023
Listing Expiration Date 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.	12-31-2024
Exclude Flag 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".	N
NDC Code Structure	44911 - Energique, Inc. 44911-0668 - Psora Miasm 44911-0668-1

Product Packages

NDC Code 44911-0668-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What are Psora Miasm 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.

ARSENIC TRIOXIDE 12 [hp_C]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
CENTELLA ASIATICA WHOLE 12 [hp_C]/mL
EGG SHELL MEMBRANE 6 [hp_X]/mL
FAGOPYRUM ESCULENTUM WHOLE 12 [hp_C]/mL
GRAPHITE 12 [hp_C]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
SODIUM CHLORIDE 12 [hp_C]/mL - A ubiquitous sodium salt that is commonly used to season food.
SULFUR 30 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
WHEY 6 [hp_X]/mL - The liquid components of milk that remain after the CASEIN, fat, and fat soluble components have been removed. It is also a byproduct of cheese production.

Pharmacologic Class(es)

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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