Ohm Hepatic Terrain

Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, China Officinalis, Cynara Scolymus, Taraxacum Officinale, Veratrum Album

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-176

Ohm Hepatic Terrain also known as Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, China Officinalis, Cynara Scolymus, Taraxacum Officinale, Veratrum Album is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Hepatic Terrain is 66096-176. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ohm Hepatic Terrain drug includes Berberis Vulgaris Root Bark - 12 [hp_X]/mL Chelidonium Majus - 12 [hp_X]/mL Cinchona Officinalis Bark - 7 [hp_X]/mL Cynara Scolymus Leaf - 9 [hp_X]/mL Milk Thistle - 6 [hp_X]/mL Taraxacum Officinale - 7 [hp_X]/mL Veratrum Album Root - 12 [hp_X]/mL . The currest status of Ohm Hepatic Terrain drug is Active.

Drug Information:

Drug NDC:	66096-176
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:	Ohm Hepatic Terrain
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:	Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, China Officinalis, Cynara Scolymus, Taraxacum Officinale, Veratrum Album
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Ohm Pharma 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:	BERBERIS VULGARIS ROOT BARK - 12 [hp_X]/mL CHELIDONIUM MAJUS - 12 [hp_X]/mL CINCHONA OFFICINALIS BARK - 7 [hp_X]/mL CYNARA SCOLYMUS LEAF - 9 [hp_X]/mL MILK THISTLE - 6 [hp_X]/mL TARAXACUM OFFICINALE - 7 [hp_X]/mL VERATRUM ALBUM ROOT - 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:	23 Apr, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	13 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:	OHM PHARMA 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:	0366096176068 0366096016241
UPC stands for Universal Product Code.
UNII:	1TH8Q20J0U 7E889U5RNN S003A158SB B71UA545DE U946SH95EE 39981FM375 QNS6W5US1Z
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
66096-176-06	12 AMPULE in 1 BOX (66096-176-06) / 2.2 mL in 1 AMPULE	23 Apr, 2015	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

Ohm Hepatic Terrain

Berberis Vulgaris & more..

Liquid
OHM PHARMA INC.
NDC: 66096-176

Ohm-hep

Berberis Vulgaris & more..

Spray
OHM PHARMA INC.
NDC: 66096-756

Purpose:

Primary and secondary functional hepatic disorders relief

Product Elements:

Ohm hepatic terrain berberis vulgaris, carduus marianus, chelidonium majus, china officinalis, cynara scolymus, taraxacum officinale, veratrum album sodium chloride berberis vulgaris root bark berberis vulgaris root bark milk thistle milk thistle chelidonium majus chelidonium majus cinchona officinalis bark cinchona officinalis bark cynara scolymus leaf cynara scolymus leaf taraxacum officinale taraxacum officinale veratrum album root veratrum album root

Indications and Usage:

Uses: temporarily relieves primary and secondary functional hepatic disorders.** **this statement has not been evaluated by the fda. it is based on documented homeopathic materia medica.

Warnings:

Warnings: if pregnant or breast-feeding, ask a health professional before use. if symptoms worsen or persist for more than 5 days, discontinue use and contact a health care professional. keep out of the reach of children.

Dosage and Administration:

Directions: to open ampoule snap top up and away from you. using pipette place entire content under the tongue, hold it for 30 seconds and swallow. posology: adults and children over 12 years: in acute conditions: 1 ampoule every 12 hours. in chronic conditions: 1 ampoule one to four times per week, or as directed by a health professional. children under 12 years use 1/2 the adult dose. discard unused solution. solution does not contain any preservatives. not for injection.

Package Label Principal Display Panel:

Ndc: 66096-176-06 ohm hepatic terrain homeopathic medicine pharmaceutical grade. professional use only. contents: 12 oral ampoules of 2.2 ml each. terrain box label english terrain box label spanish ampoule label insert english insert spanish

Further Questions:

Mfg. by: ohm pharma, inc. / mineral wells, tx 76067 made in usa www.ohmpharma.com

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.