N02 Petrochem

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

Apex Energetics Inc.
Human Otc Drug
NDC 63479-1402

N02 Petrochem also known as 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 human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for N02 Petrochem is 63479-1402. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in N02 Petrochem drug includes Acetone - 15 [hp_X]/mL Activated Charcoal - 12 [hp_X]/mL Aniline - 30 [hp_X]/mL Benzene - 15 [hp_X]/mL Benzo(a)pyrene - 30 [hp_X]/mL Carbon Tetrachloride - 15 [hp_X]/mL Ether - 12 [hp_X]/mL Kerosene - 30 [hp_X]/mL Lead - 15 [hp_X]/mL Lead Chloride - 15 [hp_X]/mL and more. The currest status of N02 Petrochem drug is Active.

Drug Information:

Drug NDC:	63479-1402
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	N02 Petrochem
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	N02
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	PETROCHEM
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary 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
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Apex Energetics Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Solution/ Drops
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACETONE - 15 [hp_X]/mL ACTIVATED CHARCOAL - 12 [hp_X]/mL ANILINE - 30 [hp_X]/mL BENZENE - 15 [hp_X]/mL BENZO(A)PYRENE - 30 [hp_X]/mL CARBON TETRACHLORIDE - 15 [hp_X]/mL ETHER - 12 [hp_X]/mL KEROSENE - 30 [hp_X]/mL LEAD - 15 [hp_X]/mL LEAD CHLORIDE - 15 [hp_X]/mL Load more... MAGNESIUM SULFATE HEPTAHYDRATE - 15 [hp_X]/mL METHYL ALCOHOL - 12 [hp_X]/mL PHENOL - 30 [hp_X]/mL PHENOLPHTHALEIN - 15 [hp_X]/mL PHOSPHORUS - 30 [hp_X]/mL PICRIC ACID - 15 [hp_X]/mL PINE TAR - 12 [hp_X]/mL SULFONMETHANE - 15 [hp_X]/mL SULFURIC ACID - 15 [hp_X]/mL TRICHLOROETHYLENE - 30 [hp_X]/mL TURPENTINE OIL - 12 [hp_X]/mL VANADIUM - 15 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	SUBLINGUAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	15 Jul, 1997
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	06 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Apex Energetics Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0818960012977
UPC stands for Universal Product Code.
UNII:	1364PS73AF 2P3VWU3H10 SIR7XX2F1K J64922108F 3417WMA06D CL2T97X0V0 0F5N573A2Y 1C89KKC04E 2P299V784P 4IL61GN3YI Load more... SK47B8698T Y4S76JWI15 339NCG44TV 6QK969R2IF 27YLU75U4W A49OS0F91S YFH4WC535J W00D22B592 O40UQP6WCF 290YE8AR51 C5H0QJ6V7F 00J9J9XKDE
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:	Calculi Dissolution Agent [EPC] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Inhibition Small Intestine Fluid/Electrolyte Absorption [PE] Magnesium Ion Exchange Activity [MoA] Osmotic Activity [MoA] Osmotic Laxative [EPC] Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
DEA Schedule:	CIII
This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
63479-1402-1	30 mL in 1 BOTTLE, GLASS (63479-1402-1)	15 Jul, 1997	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

N02 Petrochem

Acetone & more..

Solution/ Drops
Apex Energetics Inc.
NDC: 63479-1402

Purpose:

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.

Product Elements:

N02 petrochem 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 sulfuric acid sulfuric acid water acetone acetone picric acid picric acid pine tar pine tar sulfonmethane sulfonmethane vanadium vanadium alcohol activated charcoal activated charcoal aniline aniline benzene benzene phenol phenol methyl alcohol methyl alcohol kerosene kerosene phenolphthalein phenolphthalein turpentine oil turpentine oil benzo(a)pyrene benzo(a)pyrene carbon tetrachloride carbon tetrachloride trichloroethylene trichloroethylene ether ether magnesium sulfate heptahydrate magnesium cation phosphorus phosphorus lead chloride lead lead lead

Indications and Usage:

Uses: 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.

Warnings:

Warnings: if pregnant or breastfeeding , ask a health professional before use. do not use if clear seal over the cap is broken or missing. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. stop use and ask a doctor if headache, rash, muscle aches, itching, dizziness, confusion, diarrhea, or other symptoms do not improve within 7 days or are accompanied by fever.

Dosage and Administration:

Directions: adults & children ages 12 years and over: take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. consult a physician for use in children under 12 years of age.

Stop Use:

Stop use and ask a doctor if headache, rash, muscle aches, itching, dizziness, confusion, diarrhea, or other symptoms do not improve within 7 days or are accompanied by fever.

Package Label Principal Display Panel:

FutureplexÂ® n02 antitoxÂ® petrochemâ¢ homeopathic formula headache* rash* muscle aches* 1 fl oz (30 ml) alcohol 20% by volume n0221-0310

Further Questions:

Distributed by apex energetics. questions? 16592 hale ave., irvine, ca 92606, usa

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.