Isopathic Phenolic Rings Liquid
NDC 64578-0109

View dosage, usage, ingredients, routes, and UNII mappings.

Product Information

Isopathic Phenolic Rings (homeopathic liquid) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energetix Corporation. This medication is typically used as a acidifying activity [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 64578-0109 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
64578-0109
Proprietary Name:
Isopathic Phenolic Rings
Non-Proprietary Name: [1]
Homeopathic Liquid
Substance Name: [2]
Acetaldehyde; Anhydrous Citric Acid; Arabica Coffee Bean; Benzene; Bos Taurus Hypothalamus; Bos Taurus Testicle; Caffeine; Candida Albicans; Choline; Cinnamon; Cocoa; Coumarin; Estrone; Gallic Acid; Green Peppercorn; Histamine; Indole; Kerosene; Onion; Petroselinum Crispum; Phenol; Phlorizin; Phosphorus; Sucrose; Sus Scrofa Adrenal Gland; Turpentine Oil; Valerian
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Code:
64578
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
11-03-2017
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 64578-0109?

The NDC code 64578-0109 is assigned by the FDA to the product Isopathic Phenolic Rings. It is commonly known by its generic name, homeopathic liquid. This pharmaceutical product is labeled by Energetix Corporation and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 64578-0109-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are Active Ingredients of this product?

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.
  • ACETALDEHYDE 12 [hp_X]/59.1mL - A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. It is also an intermediate in the metabolism of alcohol. It has a general narcotic action and also causes irritation of mucous membranes. Large doses may cause death from respiratory paralysis.
  • ANHYDROUS CITRIC ACID 12 [hp_X]/59.1mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
  • ARABICA COFFEE BEAN 12 [hp_X]/59.1mL
  • BENZENE 12 [hp_X]/59.1mL - Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide.
  • BOS TAURUS HYPOTHALAMUS 12 [hp_X]/59.1mL
  • BOS TAURUS TESTICLE 12 [hp_X]/59.1mL
  • CAFFEINE 12 [hp_X]/59.1mL - A methylxanthine naturally occurring in some beverages and also used as a pharmacological agent. Caffeine's most notable pharmacological effect is as a central nervous system stimulant, increasing alertness and producing agitation. It also relaxes SMOOTH MUSCLE, stimulates CARDIAC MUSCLE, stimulates DIURESIS, and appears to be useful in the treatment of some types of headache. Several cellular actions of caffeine have been observed, but it is not entirely clear how each contributes to its pharmacological profile. Among the most important are inhibition of cyclic nucleotide PHOSPHODIESTERASES, antagonism of ADENOSINE RECEPTORS, and modulation of intracellular calcium handling.
  • CANDIDA ALBICANS 12 [hp_X]/59.1mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
  • CHOLINE 12 [hp_X]/59.1mL - A basic constituent of lecithin that is found in many plants and animal organs. It is important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism.
  • CINNAMON 12 [hp_X]/59.1mL
  • COCOA 12 [hp_X]/59.1mL
  • COUMARIN 12 [hp_X]/59.1mL - Synthetic or naturally occurring substances related to coumarin, the delta-lactone of coumarinic acid.
  • ESTRONE 12 [hp_X]/59.1mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
  • GALLIC ACID 12 [hp_X]/59.1mL - A colorless or slightly yellow crystalline compound obtained from nutgalls. It is used in photography, pharmaceuticals, and as an analytical reagent.
  • GREEN PEPPERCORN 12 [hp_X]/59.1mL
  • HISTAMINE 12 [hp_X]/59.1mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
  • INDOLE 12 [hp_X]/59.1mL - Benzopyrroles with the nitrogen at the number one carbon adjacent to the benzyl portion, in contrast to ISOINDOLES which have the nitrogen away from the six-membered ring.
  • KEROSENE 12 [hp_X]/59.1mL - A refined petroleum fraction used as a fuel as well as a solvent.
  • ONION 12 [hp_X]/59.1mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
  • PETROSELINUM CRISPUM 12 [hp_X]/59.1mL - A plant genus of the family APIACEAE used for flavoring food.
  • PHENOL 12 [hp_X]/59.1mL - Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
  • PHLORIZIN 12 [hp_X]/59.1mL - A multifunctional protein that contains two enzyme domains. The first domain (EC 3.2.1.62) hydrolyzes glycosyl-N-acylsphingosine to a sugar and N-acylsphingosine. The second domain (EC 3.2.1.108) hydrolyzes LACTOSE and is found in the intestinal brush border membrane. Loss of activity for this enzyme in humans results in LACTOSE INTOLERANCE.
  • PHOSPHORUS 12 [hp_X]/59.1mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • SUCROSE 12 [hp_X]/59.1mL - A nonreducing disaccharide composed of GLUCOSE and FRUCTOSE linked via their anomeric carbons. It is obtained commercially from SUGARCANE, sugar beet (BETA VULGARIS), and other plants and used extensively as a food and a sweetener.
  • SUS SCROFA ADRENAL GLAND 9 [hp_X]/59.1mL
  • TURPENTINE OIL 12 [hp_X]/59.1mL
  • VALERIAN 12 [hp_X]/59.1mL - A plant genus of the family VALERIANACEAE, order Dipsacales, subclass Asteridae, class Magnoliopsida. It is best known for the sedative use and valepotriate content of the roots. It is sometimes called Garden Heliotrope but is unrelated to true Heliotrope (HELIOTROPIUM).

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".