Ohm Sore Throat

Aconitum Nap, Ailanthus, Baptisia, Belladonna, Ferrum Phos, Hepar Sulph Calc, Hydrastis, Merc Cyan, Merc Iod Rub, Phytolacca.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-154

Ohm Sore Throat also known as Aconitum Nap, Ailanthus, Baptisia, Belladonna, Ferrum Phos, Hepar Sulph Calc, Hydrastis, Merc Cyan, Merc Iod Rub, Phytolacca. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Sore Throat is 66096-154. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Ohm Sore Throat drug includes Aconitum Napellus - 7 [hp_X]/59mL Ailanthus Altissima Flowering Twig - 16 [hp_X]/59mL Atropa Belladonna - 7 [hp_X]/59mL Baptisia Tinctoria - 3 [hp_X]/59mL Calcium Sulfide - 12 [hp_C]/59mL Ferrosoferric Phosphate - 6 [hp_X]/59mL Goldenseal - 3 [hp_X]/59mL Mercuric Cyanide - 16 [hp_X]/59mL Mercuric Iodide - 8 [hp_X]/59mL Phytolacca Americana Root - 3 [hp_X]/59mL . The currest status of Ohm Sore Throat drug is Active.

Drug Information:

Drug NDC:	66096-154
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 Sore Throat
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:	Aconitum Nap, Ailanthus, Baptisia, Belladonna, Ferrum Phos, Hepar Sulph Calc, Hydrastis, Merc Cyan, Merc Iod Rub, Phytolacca.
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:	Spray
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:	ACONITUM NAPELLUS - 7 [hp_X]/59mL AILANTHUS ALTISSIMA FLOWERING TWIG - 16 [hp_X]/59mL ATROPA BELLADONNA - 7 [hp_X]/59mL BAPTISIA TINCTORIA - 3 [hp_X]/59mL CALCIUM SULFIDE - 12 [hp_C]/59mL FERROSOFERRIC PHOSPHATE - 6 [hp_X]/59mL GOLDENSEAL - 3 [hp_X]/59mL MERCURIC CYANIDE - 16 [hp_X]/59mL MERCURIC IODIDE - 8 [hp_X]/59mL PHYTOLACCA AMERICANA ROOT - 3 [hp_X]/59mL
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:	10 Apr, 2017
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:	0366096154059
UPC stands for Universal Product Code.
UNII:	U0NQ8555JD 8P29O5P7XU WQZ3G9PF0H 5K1UO2888Y 1MBW07J51Q 91GQH8I5F7 ZW3Z11D0JV RWG7BD1032 R03O05RB0P 11E6VI8VEG
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
66096-154-05	59 mL in 1 BOTTLE, SPRAY (66096-154-05)	10 Apr, 2017	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 Sore Throat

Aconitum Nap & more..

Spray
OHM PHARMA INC.
NDC: 66096-154

Purpose:

Relief from sore throat.

Product Elements:

Ohm sore throat aconitum nap, ailanthus, baptisia, belladonna, ferrum phos, hepar sulph calc, hydrastis, merc cyan, merc iod rub, phytolacca. alcohol water glycerin aconitum napellus aconitum napellus ailanthus altissima flowering twig ailanthus altissima flowering twig baptisia tinctoria baptisia tinctoria atropa belladonna atropa belladonna ferrosoferric phosphate ferrosoferric phosphate calcium sulfide calcium sulfide goldenseal goldenseal mercuric cyanide mercuric cyanide mercuric iodide mercuric iodide phytolacca americana root phytolacca americana root

Indications and Usage:

Uses: temporarily relieves symptoms caused by common throat irritation.** 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 professional before use. severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomitting may be serious. consult a physician promptly. do not use for more than 2 days or administer to children under 3 years of age unless directed by a physician. 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 every 15 minutes, extend intervals as symptoms improve or as directed by a health care professional. children under 12 years: use half the adult dose.

Package Label Principal Display Panel:

Homeopathic medicine ndc: 66096-154-05 sore throat natural - safe - effective no side effects 2 fl oz (59 ml) / 15% alcohol product of usa 2oz bottle label relief from sore throat.

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.