Ohm Sinus Nasal

Aralia Rac, Euphorbium, Galphimia, Hepar Sulph Calc, Histaminum, Hydrastis, Kali Bic, Kali Iod, Luffa, Pulsatilla, Teucrium Mar.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-527

Ohm Sinus Nasal also known as Aralia Rac, Euphorbium, Galphimia, Hepar Sulph Calc, Histaminum, Hydrastis, Kali Bic, Kali Iod, Luffa, Pulsatilla, Teucrium Mar. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Sinus Nasal is 66096-527. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Ohm Sinus Nasal drug includes Anemone Pulsatilla - 6 [hp_X]/30mL Aralia Racemosa Root - 6 [hp_X]/30mL Calcium Sulfide - 12 [hp_X]/30mL Euphorbia Resinifera Resin - 6 [hp_X]/30mL Galphimia Glauca Flowering Top - 6 [hp_X]/30mL Goldenseal - 12 [hp_X]/30mL Histamine Dihydrochloride - 12 [hp_X]/30mL Luffa Operculata Fruit - 6 [hp_X]/30mL Potassium Dichromate - 12 [hp_X]/30mL Potassium Iodide - 4 [hp_X]/30mL and more. The currest status of Ohm Sinus Nasal drug is Active.

Drug Information:

Drug NDC:	66096-527
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 Sinus Nasal
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:	Aralia Rac, Euphorbium, Galphimia, Hepar Sulph Calc, Histaminum, Hydrastis, Kali Bic, Kali Iod, Luffa, Pulsatilla, Teucrium Mar.
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:	ANEMONE PULSATILLA - 6 [hp_X]/30mL ARALIA RACEMOSA ROOT - 6 [hp_X]/30mL CALCIUM SULFIDE - 12 [hp_X]/30mL EUPHORBIA RESINIFERA RESIN - 6 [hp_X]/30mL GALPHIMIA GLAUCA FLOWERING TOP - 6 [hp_X]/30mL GOLDENSEAL - 12 [hp_X]/30mL HISTAMINE DIHYDROCHLORIDE - 12 [hp_X]/30mL LUFFA OPERCULATA FRUIT - 6 [hp_X]/30mL POTASSIUM DICHROMATE - 12 [hp_X]/30mL POTASSIUM IODIDE - 4 [hp_X]/30mL Load more... TEUCRIUM MARUM - 6 [hp_X]/30mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	NASAL
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 Jan, 2017
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	25 Dec, 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:	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:	0366096527099
UPC stands for Universal Product Code.
UNII:	I76KB35JEV T90W4582DU 1MBW07J51Q 1TI1O9028K 93PH5Q8M7E ZW3Z11D0JV 3POA0Q644U C4MO6809HU T4423S18FM 1C4QK22F9J Load more... 10464S0TAA
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
66096-527-09	30 mL in 1 BOTTLE, SPRAY (66096-527-09)	23 Jan, 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 Sinus Nasal

Aralia Rac & more..

Spray
OHM PHARMA INC.
NDC: 66096-527

Purpose:

Allergy / sinus relief.

Product Elements:

Ohm sinus nasal aralia rac, euphorbium, galphimia, hepar sulph calc, histaminum, hydrastis, kali bic, kali iod, luffa, pulsatilla, teucrium mar. benzalkonium chloride water sodium chloride aralia racemosa root aralia racemosa root euphorbia resinifera resin euphorbia resinifera resin galphimia glauca flowering top galphimia glauca flowering top calcium sulfide calcium sulfide histamine dihydrochloride histamine goldenseal goldenseal potassium dichromate dichromate ion potassium iodide iodide ion luffa operculata fruit luffa operculata fruit anemone pulsatilla anemone pulsatilla teucrium marum teucrium marum

Indications and Usage:

Uses: temporarily relieves symptoms associated with allergy and sinus.** 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. 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 and children over 6: 1-2 sprays into each nostril, 4-6 times daily. children under 6: 1 spray, 3-4 times daily.

Package Label Principal Display Panel:

Homeopathic medicine ndc: 66096-527-09 sinus nasal spray natural - safe - effective no side effects 1 fl oz (30 ml) product of usa 1oz bottle label allergy / sinus relief.

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.