Parastat

Artemisia Vulgaris, Cina, Sabadilla, Spigelia Anthelmia, Filix Mas, Baryta Carbonica, Calcarea Carbonica, Sulphur, Terebinthina

Energique, Inc.
Human Otc Drug
NDC 44911-0487

Parastat also known as Artemisia Vulgaris, Cina, Sabadilla, Spigelia Anthelmia, Filix Mas, Baryta Carbonica, Calcarea Carbonica, Sulphur, Terebinthina is a human otc drug labeled by 'Energique, Inc.'. National Drug Code (NDC) number for Parastat is 44911-0487. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Parastat drug includes Artemisia Cina Pre-flowering Top - 3 [hp_X]/mL Artemisia Vulgaris Root - 3 [hp_X]/mL Barium Carbonate - 12 [hp_X]/mL Dryopteris Filix-mas Root - 4 [hp_X]/mL Oyster Shell Calcium Carbonate, Crude - 12 [hp_X]/mL Schoenocaulon Officinale Seed - 3 [hp_X]/mL Spigelia Anthelmia - 3 [hp_X]/mL Sulfur - 12 [hp_X]/mL Turpentine Oil - 12 [hp_X]/mL . The currest status of Parastat drug is Active.

Drug Information:

Drug NDC:	44911-0487
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:	Parastat
Also known as the trade name. It is the name of the product chosen by the labeler.
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:	Artemisia Vulgaris, Cina, Sabadilla, Spigelia Anthelmia, Filix Mas, Baryta Carbonica, Calcarea Carbonica, Sulphur, Terebinthina
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Energique, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
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:	ARTEMISIA CINA PRE-FLOWERING TOP - 3 [hp_X]/mL ARTEMISIA VULGARIS ROOT - 3 [hp_X]/mL BARIUM CARBONATE - 12 [hp_X]/mL DRYOPTERIS FILIX-MAS ROOT - 4 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 12 [hp_X]/mL SCHOENOCAULON OFFICINALE SEED - 3 [hp_X]/mL SPIGELIA ANTHELMIA - 3 [hp_X]/mL SULFUR - 12 [hp_X]/mL TURPENTINE OIL - 12 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
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:	01 Feb, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	20 Apr, 2025
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:	23 Dec, 2025
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:	Energique, 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:	0363113700534
UPC stands for Universal Product Code.
UNII:	28M1820ACT 32MP823R8S 6P669D8HQ8 C0ZK0RRF5X 2E32821G6I 6NAF1689IO WYT05213GE 70FD1KFU70 C5H0QJ6V7F
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
44911-0487-1	30 mL in 1 BOTTLE, DROPPER (44911-0487-1)	01 Feb, 2019	20 Apr, 2025	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

Parastat

Artemisia Vulgaris & more..

Liquid
Energique, Inc.
NDC: 44911-0487

Purpose:

Indications: may temporarily relieve itching of anus, colic, bloating, pain and constipation.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Parastat artemisia vulgaris, cina, sabadilla, spigelia anthelmia, filix mas, baryta carbonica, calcarea carbonica, sulphur, terebinthina artemisia vulgaris root artemisia vulgaris root artemisia cina pre-flowering top artemisia cina flower schoenocaulon officinale seed schoenocaulon officinale seed spigelia anthelmia spigelia anthelmia dryopteris filix-mas root dryopteris filix-mas root barium carbonate barium cation oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude sulfur sulfur turpentine oil turpentine oil water alcohol

Indications and Usage:

Indications: may temporarily relieve itching of anus, colic, bloating, pain and constipation.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. do not use if tamper evident seal is broken or missing. store in a cool, dry place.

Dosage and Administration:

Directions: adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. if symptoms persist for more than 7 days, consult your health care professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: energique since 1987 homeopathic remedy parastat 1 fl. oz. (30 ml) parastat

Further Questions:

Questions: dist. by energique, inc. 201 apple blvd woodbine, ia 51579 800.869.8078

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.