Ohm Flu

Anas Barbariae, Hepatis Et Cordis Extractum, Influenzinum

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-170

Ohm Flu also known as Anas Barbariae, Hepatis Et Cordis Extractum, Influenzinum is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Flu is 66096-170. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ohm Flu drug includes Cairina Moschata Heart/liver Autolysate - 200 [hp_C]/mL Influenza A Virus - 9 [hp_C]/mL Influenza B Virus - 9 [hp_C]/mL . The currest status of Ohm Flu drug is Active.

Drug Information:

Drug NDC:	66096-170
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 Flu
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:	Anas Barbariae, Hepatis Et Cordis Extractum, Influenzinum
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:	CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE - 200 [hp_C]/mL INFLUENZA A VIRUS - 9 [hp_C]/mL INFLUENZA B VIRUS - 9 [hp_C]/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:	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:	0366096016241 0366096170066
UPC stands for Universal Product Code.
UNII:	RN2HC612GY R9HH0NDE2E 1314JZ2X6W
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
66096-170-06	12 AMPULE in 1 BOX (66096-170-06) / 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 Flu

Anas Barbariae, Hepatis Et Cordis Extractum, Influenzinum

Liquid
OHM PHARMA INC.
NDC: 66096-170

Purpose:

Flu, fever, congestion, body aches and pains relief

Product Elements:

Ohm flu anas barbariae, hepatis et cordis extractum, influenzinum sodium chloride cairina moschata heart/liver autolysate cairina moschata heart/liver autolysate influenza a virus influenza a virus influenza b virus influenza b virus

Indications and Usage:

Uses: temporarily relieves relieves fever, congestion, body aches and pains. to help reduce and prevent the development of flu symptoms.** **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 persist for more than 3 days, discontinue use and contact a health professional. this product is not intended to be an alternative to vaccination. 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. flu prevention protocal: adults and children over 6 years: take 1 ampoule every week for six weeks. flu treatment protocol: take 1 dose at the first sign of flu or 1 dose every 12 hours according to symptoms. children under 6 years old: use half the adult dose. children under 2: consult a health professional before use. discard unused solution. solution does not contain any preservatives. not for injection.

Package Label Principal Display Panel:

Ndc: 66096-170-06 ohm flu homeopathic medicine pharmaceutical grade. professional use only. contents: 12 oral ampoules of 2.2 ml each. terrain box english terrain box spanish ampoule box 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.