Lipotox Liquid
NDC 43857-0636

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0636?
  4. Lipotox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Lipotox (squalene, cholesterinum, estradiol, progesterone, aspartame, benzalkonium chloride, formalinum, methylene chloride, methylparaben, propylparaben, sodium benzoate, sodium citrate, titanium dioxide, zincum oxydatum, arsenicum album, lycopodium clavatum, nux vomica, phosphoricum acidum, phosphorus, aceticum acidum, benzoicum acidum, benzyl alcohol, boricum acidum, chlorinum, cortisone aceticum, eugenol, folliculinum, isopropyl palmitate, lacticum acidum, petroleum jelly, phenyl butazone, plumbum metallicum,) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bioactive Nutritional, Inc.. 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 43857-0636 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43857-0636
Proprietary Name:
Lipotox
Non-Proprietary Name: [1]
Squalene, Cholesterinum, Estradiol, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methylparaben, Propylparaben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Aceticum Acidum, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly, Phenyl Butazone, Plumbum Metallicum,
Substance Name: [2]
Acetic Acid; Anhydrous Trisodium Citrate; Arsenic Trioxide; Aspartame; Benzalkonium Chloride; Benzoic Acid; Benzyl Alcohol; Boric Acid; Chlorine; Cholesterol; Corticotropin; Cortisone Acetate; Estradiol; Estrone; Eugenol; Formaldehyde Solution; Isopropyl Palmitate; Lactic Acid, Dl-; Lead; Lycopodium Clavatum Spore; Methylene Chloride; Methylparaben; Petrolatum; Phenylbutazone; Phosphoric Acid; Phosphorus; Potassium Sorbate; Progesterone; Propylparaben; Resorcinol; Salicylic Acid; Sodium Benzoate; Sorbitol; Squalene; Stearyl Alcohol; Strychnos Nux-vomica Seed; Titanium Dioxide; Xylitol; Zinc Oxide
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]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
a1538692-ca00-4e52-9b7e-409767ee27e1
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-05-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43857-0636?

The NDC code 43857-0636 is assigned by the FDA to the product Lipotox. It is commonly known by its generic name, squalene, cholesterinum, estradiol, progesterone, aspartame, benzalkonium chloride, formalinum, methylene chloride, methylparaben, propylparaben, sodium benzoate, sodium citrate, titanium dioxide, zincum oxydatum, arsenicum album, lycopodium clavatum, nux vomica, phosphoricum acidum, phosphorus, aceticum acidum, benzoicum acidum, benzyl alcohol, boricum acidum, chlorinum, cortisone aceticum, eugenol, folliculinum, isopropyl palmitate, lacticum acidum, petroleum jelly, phenyl butazone, plumbum metallicum, . This pharmaceutical product is labeled by Bioactive Nutritional, Inc. 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: 43857-0636-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

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.
  • ACETIC ACID 30 [hp_X]/mL - 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)
  • ANHYDROUS TRISODIUM CITRATE 30 [hp_X]/mL
  • ARSENIC TRIOXIDE 30 [hp_X]/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.
  • ASPARTAME 30 [hp_X]/mL - Flavoring agent sweeter than sugar, metabolized as PHENYLALANINE and ASPARTIC ACID.
  • BENZALKONIUM CHLORIDE 30 [hp_X]/mL
  • BENZOIC ACID 30 [hp_X]/mL - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
  • BENZYL ALCOHOL 30 [hp_X]/mL - Alcohols derived from the aryl radical (C6H5CH2-) and defined by C6H5CHOH. The concept includes derivatives with any substituents on the benzene ring.
  • BORIC ACID 30 [hp_X]/mL - Inorganic and organic derivatives of boric acid either B(OH)3 or, preferably H3BO3.
  • CHLORINE 30 [hp_X]/mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
  • CHOLESTEROL 12 [hp_X]/mL - The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
  • CORTICOTROPIN 30 [hp_C]/mL
  • CORTISONE ACETATE 30 [hp_X]/mL - 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)
  • ESTRADIOL 12 [hp_X]/mL - The 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl group at 3-beta- and 17-beta-position. Estradiol-17-beta is the most potent form of mammalian estrogenic steroids.
  • ESTRONE 30 [hp_X]/mL - 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.
  • EUGENOL 30 [hp_X]/mL - A cinnamate derivative of the shikimate pathway found in CLOVE OIL and other PLANTS.
  • FORMALDEHYDE SOLUTION 30 [hp_X]/mL
  • ISOPROPYL PALMITATE 30 [hp_X]/mL
  • LACTIC ACID, DL- 30 [hp_X]/mL
  • LEAD 30 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
  • METHYLENE CHLORIDE 30 [hp_X]/mL - A chlorinated hydrocarbon that has been used as an inhalation anesthetic and acts as a narcotic in high concentrations. Its primary use is as a solvent in manufacturing and food technology.
  • METHYLPARABEN 30 [hp_X]/mL - used as a preservative in cosmetics but potentiates UV-induced damage of skin; RN given refers to parent cpd
  • PETROLATUM 30 [hp_X]/mL - A colloidal system of semisolid hydrocarbons obtained from PETROLEUM. It is used as an ointment base, topical protectant, and lubricant.
  • PHENYLBUTAZONE 30 [hp_X]/mL - A butyl-diphenyl-pyrazolidinedione that has anti-inflammatory, antipyretic, and analgesic activities. It has been used in ANKYLOSING SPONDYLITIS; RHEUMATOID ARTHRITIS; and REACTIVE ARTHRITIS.
  • PHOSPHORIC ACID 30 [hp_X]/mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • PHOSPHORUS 30 [hp_X]/mL - 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.
  • POTASSIUM SORBATE 30 [hp_X]/mL - Mold and yeast inhibitor. Used as a fungistatic agent for foods, especially cheeses.
  • PROGESTERONE 12 [hp_X]/mL - The major progestational steroid that is secreted primarily by the CORPUS LUTEUM and the PLACENTA. Progesterone acts on the UTERUS, the MAMMARY GLANDS and the BRAIN. It is required in EMBRYO IMPLANTATION; PREGNANCY maintenance, and the development of mammary tissue for MILK production. Progesterone, converted from PREGNENOLONE, also serves as an intermediate in the biosynthesis of GONADAL STEROID HORMONES and adrenal CORTICOSTEROIDS.
  • PROPYLPARABEN 30 [hp_X]/mL - RN given refers to cpd with hydroxy group locant in position 4; structure
  • RESORCINOL 30 [hp_X]/mL - A water-soluble crystalline benzene-1,3-diol (resorcinol) and its derivatives.
  • SALICYLIC ACID 30 [hp_X]/mL - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
  • SODIUM BENZOATE 30 [hp_X]/mL - The sodium salt of BENZOIC ACID. It is used as an antifungal preservative in pharmaceutical preparations and foods. It may also be used as a test for liver function.
  • SORBITOL 30 [hp_X]/mL - A polyhydric alcohol with about half the sweetness of sucrose. Sorbitol occurs naturally and is also produced synthetically from glucose. It was formerly used as a diuretic and may still be used as a laxative and in irrigating solutions for some surgical procedures. It is also used in many manufacturing processes, as a pharmaceutical aid, and in several research applications.
  • SQUALENE 8 [hp_X]/mL - A natural 30-carbon triterpene.
  • STEARYL ALCOHOL 30 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL
  • TITANIUM DIOXIDE 30 [hp_X]/mL - used medically as protectant against externally caused irritation & sunlight; high concentrations of dust may cause irritation to respiratory tract; RN given refers to titanium oxide (TiO2); structure
  • XYLITOL 30 [hp_X]/mL - A five-carbon sugar alcohol derived from XYLOSE by reduction of the carbonyl group. It is as sweet as sucrose and used as a noncariogenic sweetener.
  • ZINC OXIDE 30 [hp_X]/mL - A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.

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.

* Please review the full disclaimer at the bottom of this page.

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".