Aller-chord F Liquid
NDC 64578-0148

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 64578-0148?
  4. Active Ingredients
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Pharmacologic Classes

Product Information

Aller-chord F (acetaldehyde, aceticum ac, arg nit, caffeinum, calc sulph, citricum ac, cortisone aceticum, echinacea purp, folliculinum, fragaria, fumaricum ac, gallicum ac, glandula suprarenalis suis, hepar suis, histaminum hydrochloricum, hydrangea, lac vac, lecithin, limulus, lycopersicum, lycopodium, nat bicarb, nat mur, nux vom, paraffinum, phosphoricum ac, saccharum off, silicea, tartaricum ac, torula cerevisiae.) 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 64578-0148 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
64578-0148
Proprietary Name:
Aller-chord F
Non-Proprietary Name: [1]
Acetaldehyde, Aceticum Ac, Arg Nit, Caffeinum, Calc Sulph, Citricum Ac, Cortisone Aceticum, Echinacea Purp, Folliculinum, Fragaria, Fumaricum Ac, Gallicum Ac, Glandula Suprarenalis Suis, Hepar Suis, Histaminum Hydrochloricum, Hydrangea, Lac Vac, Lecithin, Limulus, Lycopersicum, Lycopodium, Nat Bicarb, Nat Mur, Nux Vom, Paraffinum, Phosphoricum Ac, Saccharum Off, Silicea, Tartaricum Ac, Torula Cerevisiae.
Substance Name: [2]
Acetaldehyde; Acetic Acid; Alpine Strawberry; Anhydrous Citric Acid; Caffeine; Calcium Sulfate Anhydrous; Cortisone Acetate; Cow Milk; Echinacea Purpurea; Egg Phospholipids; Estrone; Fumaric Acid; Gallic Acid Monohydrate; Histamine Dihydrochloride; Hydrangea Arborescens Root; Limulus Polyphemus; Lycopodium Clavatum Spore; Paraffin; Phosphoric Acid; Pork Liver; Saccharomyces Cerevisiae; Silicon Dioxide; Silver Nitrate; Sodium Bicarbonate; Sodium Chloride; Solanum Lycopersicum; Strychnos Nux-vomica Seed; Sucrose; Sus Scrofa Adrenal Gland; Tartaric Acid
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 Name: [5]
Energetix Corporation
Labeler Code:
64578
Product Label ID:
ff4eb7b2-8272-4bd3-99a9-7e589b30d59a
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
08-08-2014
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 64578-0148?

The NDC code 64578-0148 is assigned by the FDA to the product Aller-chord F. It is commonly known by its generic name, acetaldehyde, aceticum ac, arg nit, caffeinum, calc sulph, citricum ac, cortisone aceticum, echinacea purp, folliculinum, fragaria, fumaricum ac, gallicum ac, glandula suprarenalis suis, hepar suis, histaminum hydrochloricum, hydrangea, lac vac, lecithin, limulus, lycopersicum, lycopodium, nat bicarb, nat mur, nux vom, paraffinum, phosphoricum ac, saccharum off, silicea, tartaricum ac, torula cerevisiae.. 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: 64578-0148-1. 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.
  • ACETIC ACID 15 [hp_X]/59.1mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
  • ALPINE STRAWBERRY 15 [hp_X]/59.1mL - A plant genus of the family ROSACEAE known for the edible fruit.
  • ANHYDROUS CITRIC ACID 15 [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.
  • CAFFEINE 15 [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.
  • CALCIUM SULFATE ANHYDROUS 15 [hp_X]/59.1mL
  • CORTISONE ACETATE 20 [hp_X]/59.1mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
  • COW MILK 15 [hp_X]/59.1mL - The off-white liquid secreted by the mammary glands of humans and other mammals. It contains proteins, sugar, lipids, vitamins, and minerals.
  • ECHINACEA PURPUREA 6 [hp_X]/59.1mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
  • EGG PHOSPHOLIPIDS 15 [hp_X]/59.1mL
  • ESTRONE 15 [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.
  • FUMARIC ACID 15 [hp_X]/59.1mL - see also record for ferrous fumarate; use FUMARATES for general fumaric acid esters
  • GALLIC ACID MONOHYDRATE 12 [hp_X]/59.1mL
  • HISTAMINE DIHYDROCHLORIDE 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.
  • HYDRANGEA ARBORESCENS ROOT 6 [hp_X]/59.1mL
  • LIMULUS POLYPHEMUS 15 [hp_X]/59.1mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/59.1mL
  • PARAFFIN 15 [hp_X]/59.1mL - A mixture of solid hydrocarbons obtained from petroleum. It has a wide range of uses including as a stiffening agent in ointments, as a lubricant, and as a topical anti-inflammatory. It is also commonly used as an embedding material in histology.
  • PHOSPHORIC ACID 15 [hp_X]/59.1mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • PORK LIVER 9 [hp_X]/59.1mL
  • SACCHAROMYCES CEREVISIAE 15 [hp_X]/59.1mL - A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as baker's or brewer's yeast. The dried form is used as a dietary supplement.
  • SILICON DIOXIDE 15 [hp_X]/59.1mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
  • SILVER NITRATE 10 [hp_X]/59.1mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
  • SODIUM BICARBONATE 15 [hp_X]/59.1mL - A white, crystalline powder that is commonly used as a pH buffering agent, an electrolyte replenisher, systemic alkalizer and in topical cleansing solutions.
  • SODIUM CHLORIDE 12 [hp_X]/59.1mL - A ubiquitous sodium salt that is commonly used to season food.
  • SOLANUM LYCOPERSICUM 15 [hp_X]/59.1mL - A plant species of the family SOLANACEAE, native of South America, widely cultivated for their edible, fleshy, usually red fruit.
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/59.1mL
  • SUCROSE 15 [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
  • TARTARIC ACID 15 [hp_X]/59.1mL - RN given refers to cpd with unspecified isomeric designation

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?

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 & 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".