N02 Solution/ Drops
NDC 63479-1402

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 63479-1402?
  4. N02 Petrochem Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

N02 (acetone, anilinum, benzinum, benzopyrene, carbo vegetabilis, carbolicum acidum, carbon tetrachloride, ether, magnesia sulphurica, methyl alcohol, petroleum, phenolphthalein, phosphorus, picricum acidum, pine tar, plumbous chloride, plumbum metallicum, sulphonalum, sulphuricum acidum, terebinthina, trichloroethylene, vanadium metallicum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Apex Energetics Inc.. This medication is typically used as a calculi dissolution agent [epc]. It is supplied as a solution/ drops for sublingual administration. This product entry covers the primary NDC 63479-1402 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
63479-1402
Proprietary Name:
N02 Petrochem
Non-Proprietary Name: [1]
Acetone, Anilinum, Benzinum, Benzopyrene, Carbo Vegetabilis, Carbolicum Acidum, Carbon Tetrachloride, Ether, Magnesia Sulphurica, Methyl Alcohol, Petroleum, Phenolphthalein, Phosphorus, Picricum Acidum, Pine Tar, Plumbous Chloride, Plumbum Metallicum, Sulphonalum, Sulphuricum Acidum, Terebinthina, Trichloroethylene, Vanadium Metallicum
Substance Name: [2]
Sulfuric Acid; Acetone; Picric Acid; Pine Tar; Sulfonmethane; Vanadium; Activated Charcoal; Aniline; Benzene; Phenol; Methyl Alcohol; Kerosene; Phenolphthalein; Turpentine Oil; Benzo(a)pyrene; Carbon Tetrachloride; Trichloroethylene; Ether; Magnesium Sulfate Heptahydrate; Phosphorus; Lead Chloride; Lead
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
Sublingual - Administration beneath the tongue.

Labeler & Regulatory Data

Labeler Name: [5]
Apex Energetics Inc.
Labeler Code:
63479
Product Label ID:
ba5e7801-667b-ab7c-e053-2995a90a788c
DEA Schedule: [7]
Schedule III (CIII) Substances
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-15-1997
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 63479-1402?

The NDC code 63479-1402 is assigned by the FDA to the product N02 Petrochem. It is commonly known by its generic name, acetone, anilinum, benzinum, benzopyrene, carbo vegetabilis, carbolicum acidum, carbon tetrachloride, ether, magnesia sulphurica, methyl alcohol, petroleum, phenolphthalein, phosphorus, picricum acidum, pine tar, plumbous chloride, plumbum metallicum, sulphonalum, sulphuricum acidum, terebinthina, trichloroethylene, vanadium metallicum. This pharmaceutical product is labeled by Apex Energetics Inc. and is currently categorized as listed product. The medication is a solution/ drops administered via sublingual route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63479-1402-1. 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?

This product is used as Uses: For temporary relief of minor: headache*rash*muscle aches*itching*dizziness*confusion*diarrhea**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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.
  • SULFURIC ACID 15 [hp_X]/mL - Inorganic and organic derivatives of sulfuric acid (H2SO4). The salts and esters of sulfuric acid are known as SULFATES and SULFURIC ACID ESTERS respectively.
  • ACETONE 12 [hp_X]/mL - A colorless liquid used as a solvent and an antiseptic. It is one of the ketone bodies produced during ketoacidosis.
  • PICRIC ACID 30 [hp_X]/mL - used as antiseptic, astringent & stimulant for epitheliazation; structure
  • PINE TAR 15 [hp_X]/mL
  • SULFONMETHANE 30 [hp_X]/mL
  • VANADIUM 15 [hp_X]/mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • ANILINE 30 [hp_X]/mL - RN given refers to parent cpd
  • BENZENE 15 [hp_X]/mL - 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.
  • PHENOL 15 [hp_X]/mL - Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
  • METHYL ALCOHOL 15 [hp_X]/mL - A colorless, flammable liquid used in the manufacture of FORMALDEHYDE and ACETIC ACID, in chemical synthesis, antifreeze, and as a solvent. Ingestion of methanol is toxic and may cause blindness.
  • KEROSENE 12 [hp_X]/mL - A refined petroleum fraction used as a fuel as well as a solvent.
  • PHENOLPHTHALEIN 30 [hp_X]/mL - A family of 3,3-bis(p-hydroxyphenyl)phthalides. They are used as CATHARTICS, indicators, and COLORING AGENTS.
  • TURPENTINE OIL 15 [hp_X]/mL
  • BENZO(A)PYRENE 30 [hp_X]/mL - A potent mutagen and carcinogen. It is a public health concern because of its possible effects on industrial workers, as an environmental pollutant, an as a component of tobacco smoke.
  • CARBON TETRACHLORIDE 15 [hp_X]/mL - A solvent for oils, fats, lacquers, varnishes, rubber waxes, and resins, and a starting material in the manufacturing of organic compounds. Poisoning by inhalation, ingestion or skin absorption is possible and may be fatal. (Merck Index, 11th ed)
  • TRICHLOROETHYLENE 12 [hp_X]/mL - A highly volatile inhalation anesthetic used mainly in short surgical procedures where light anesthesia with good analgesia is required. It is also used as an industrial solvent. Prolonged exposure to high concentrations of the vapor can lead to cardiotoxicity and neurological impairment.
  • ETHER 15 [hp_X]/mL - A mobile, very volatile, highly flammable liquid used as an inhalation anesthetic and as a solvent for waxes, fats, oils, perfumes, alkaloids, and gums. It is mildly irritating to skin and mucous membranes.
  • MAGNESIUM SULFATE HEPTAHYDRATE 15 [hp_X]/mL
  • 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.
  • LEAD CHLORIDE 12 [hp_X]/mL - RN in 9th CI Form Index for cotunnite: 14639-87-3; RN given refers to cpd with MF of Pb-Cl2
  • LEAD 15 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.

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 DEA Schedule? This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.
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".