Eczema Relief

Arsenicum Iodatum, Kali Bromatum, Kali Muriaticum, Natrum Bromatum, Niccolum Sulphuricum, Sulphur Iodatum, Viola Tricolor, Zincum Bromatum.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-192

Eczema Relief also known as Arsenicum Iodatum, Kali Bromatum, Kali Muriaticum, Natrum Bromatum, Niccolum Sulphuricum, Sulphur Iodatum, Viola Tricolor, Zincum Bromatum. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Eczema Relief is 66096-192. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Eczema Relief drug includes Arsenic Triiodide - 8 [hp_X]/59mL Nickel Sulfate Hexahydrate - 5 [hp_X]/59mL Potassium Bromide - 4 [hp_X]/59mL Potassium Chloride - 4 [hp_X]/59mL Sodium Bromide - 4 [hp_X]/59mL Sulfur Iodide - 14 [hp_X]/59mL Viola Tricolor - 12 [hp_X]/59mL Zinc Bromide - 6 [hp_X]/59mL . The currest status of Eczema Relief drug is Active.

Drug Information:

Drug NDC:	66096-192
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:	Eczema Relief
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:	Arsenicum Iodatum, Kali Bromatum, Kali Muriaticum, Natrum Bromatum, Niccolum Sulphuricum, Sulphur Iodatum, Viola Tricolor, Zincum Bromatum.
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:	ARSENIC TRIIODIDE - 8 [hp_X]/59mL NICKEL SULFATE HEXAHYDRATE - 5 [hp_X]/59mL POTASSIUM BROMIDE - 4 [hp_X]/59mL POTASSIUM CHLORIDE - 4 [hp_X]/59mL SODIUM BROMIDE - 4 [hp_X]/59mL SULFUR IODIDE - 14 [hp_X]/59mL VIOLA TRICOLOR - 12 [hp_X]/59mL ZINC BROMIDE - 6 [hp_X]/59mL
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:	22 May, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 Jun, 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:	0366096192051
UPC stands for Universal Product Code.
UNII:	3029988O2T JC9WZ4FK68 OSD78555ZM 660YQ98I10 LC1V549NOM L6L8KA2AA0 9Q24RAI43V OO7ZBU9703
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:	Copper Absorption Inhibitor [EPC] Decreased Copper Ion Absorption [PE] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Osmotic Activity [MoA] Osmotic Laxative [EPC] Potassium Compounds [CS] Potassium Salt [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
66096-192-05	59 mL in 1 PACKAGE (66096-192-05)	22 May, 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

Eczema Relief

Arsenicum Iodatum & more..

Liquid
OHM PHARMA INC.
NDC: 66096-192

Purpose:

Temporarily relieves eczema.

Product Elements:

Eczema relief arsenicum iodatum, kali bromatum, kali muriaticum, natrum bromatum, niccolum sulphuricum, sulphur iodatum, viola tricolor, zincum bromatum. alcohol water glycerin arsenic triiodide arsenic cation (3+) potassium bromide bromide ion potassium chloride potassium cation sodium bromide bromide ion nickel sulfate hexahydrate nickel cation sulfur iodide sulfur iodide viola tricolor viola tricolor zinc bromide zinc cation

Indications and Usage:

Uses: temporarily relieves eczema - psoriatic skin symptoms.** â**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 care professional before use. if symptoms worsen or persist for more than a week, discontinue use and contact a doctor. âkeep out of reach of children.

Dosage and Administration:

Directions: shake 10 times before use. adults & children above 12 years of age: spray 3-4 times under the tongue 2-3 times a day, or as directed by a health care professional. children under 12: use half the adult dose.

Package Label Principal Display Panel:

Homeopathic medicine ndc: 66096-192-05 eczema relief natural - safe - effective no side effects 2 fl oz (59 ml) / 15% alcohol product of usa 2oz bottle label temporarily relieves eczema.

Further Questions:

Mfg. by: ohm pharma, inc. mineral wells, tx 76067 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.