Allergy Relief

Allium Cepa, Apis Mellifica, Aralia Racemosa, Blatta Orientalis, Bovista, Carduus Marianus, Chelidonium Majus, Euphrasia Officinalas, Galphimia Glauca, Hedera Helix, Hydrastis Canadensis, Luffa Operculata, Nasturtium Aquaticum, Okoubaka, Sabadilla, Scrophularia Nodosa, Solidago Virgaurea, Taraxacum Officinale.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-710

Allergy Relief also known as Allium Cepa, Apis Mellifica, Aralia Racemosa, Blatta Orientalis, Bovista, Carduus Marianus, Chelidonium Majus, Euphrasia Officinalas, Galphimia Glauca, Hedera Helix, Hydrastis Canadensis, Luffa Operculata, Nasturtium Aquaticum, Okoubaka, Sabadilla, Scrophularia Nodosa, Solidago Virgaurea, Taraxacum Officinale. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Allergy Relief is 66096-710. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Allergy Relief drug includes Apis Mellifera - 5 [hp_X]/59mL Aralia Racemosa Root - 5 [hp_X]/59mL Blatta Orientalis - 12 [hp_X]/59mL Chelidonium Majus - 3 [hp_X]/59mL Euphrasia Stricta - 8 [hp_X]/59mL Galphimia Glauca Flowering Top - 5 [hp_X]/59mL Goldenseal - 5 [hp_X]/59mL Hedera Helix Flowering Twig - 5 [hp_X]/59mL Luffa Operculata Fruit - 5 [hp_X]/59mL Lycoperdon Utriforme Fruiting Body - 12 [hp_C]/59mL and more. The currest status of Allergy Relief drug is Active.

Drug Information:

Drug NDC:	66096-710
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:	Allergy 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:	Allium Cepa, Apis Mellifica, Aralia Racemosa, Blatta Orientalis, Bovista, Carduus Marianus, Chelidonium Majus, Euphrasia Officinalas, Galphimia Glauca, Hedera Helix, Hydrastis Canadensis, Luffa Operculata, Nasturtium Aquaticum, Okoubaka, Sabadilla, Scrophularia Nodosa, Solidago Virgaurea, Taraxacum Officinale.
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:	APIS MELLIFERA - 5 [hp_X]/59mL ARALIA RACEMOSA ROOT - 5 [hp_X]/59mL BLATTA ORIENTALIS - 12 [hp_X]/59mL CHELIDONIUM MAJUS - 3 [hp_X]/59mL EUPHRASIA STRICTA - 8 [hp_X]/59mL GALPHIMIA GLAUCA FLOWERING TOP - 5 [hp_X]/59mL GOLDENSEAL - 5 [hp_X]/59mL HEDERA HELIX FLOWERING TWIG - 5 [hp_X]/59mL LUFFA OPERCULATA FRUIT - 5 [hp_X]/59mL LYCOPERDON UTRIFORME FRUITING BODY - 12 [hp_C]/59mL Load more... MILK THISTLE - 3 [hp_X]/59mL NASTURTIUM OFFICINALE - 3 [hp_X]/59mL OKOUBAKA AUBREVILLEI BARK - 5 [hp_X]/59mL ONION - 5 [hp_X]/59mL SCHOENOCAULON OFFICINALE SEED - 5 [hp_X]/59mL SCROPHULARIA NODOSA - 3 [hp_X]/59mL SOLIDAGO VIRGAUREA FLOWERING TOP - 5 [hp_X]/59mL TARAXACUM OFFICINALE - 3 [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:	02 Jun, 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.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274 N0000185365 M0028968 N0000185371 M0006342 M0022575
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	7S82P3R43Z T90W4582DU 535787266D 7E889U5RNN C9642I91WL 93PH5Q8M7E ZW3Z11D0JV 3D10KUA6BM C4MO6809HU K2A74U428F Load more... U946SH95EE YH89GMV676 MK2074187Z 492225Q21H 6NAF1689IO 7H443NUB2T 5405K23S50 39981FM375
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 EPC:	Standardized Insect Venom Allergenic Extract [EPC] Non-Standardized Insect Allergenic Extract [EPC] Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Bee Venoms [CS] Insect Proteins [CS] Dietary Proteins [CS] Vegetable Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Bee Venoms [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Insect Proteins [CS] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Insect Allergenic Extract [EPC] Standardized Insect Venom Allergenic Extract [EPC] Vegetable Proteins [CS]
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
66096-710-05	59 mL in 1 BOTTLE, SPRAY (66096-710-05)	02 Jun, 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

Allergy Relief

Allium Cepa & more..

Liquid
OHM PHARMA INC.
NDC: 66096-710

Purpose:

Natural - safe - effective no side effects

Product Elements:

Allergy relief allium cepa, apis mellifica, aralia racemosa, blatta orientalis, bovista, carduus marianus, chelidonium majus, euphrasia officinalas, galphimia glauca, hedera helix, hydrastis canadensis, luffa operculata, nasturtium aquaticum, okoubaka, sabadilla, scrophularia nodosa, solidago virgaurea, taraxacum officinale. alcohol glycerin water onion onion apis mellifera apis mellifera aralia racemosa root aralia racemosa root blatta orientalis blatta orientalis lycoperdon utriforme fruiting body lycoperdon utriforme fruiting body milk thistle milk thistle chelidonium majus chelidonium majus euphrasia stricta euphrasia stricta galphimia glauca flowering top galphimia glauca flowering top hedera helix flowering twig hedera helix flowering twig goldenseal goldenseal luffa operculata fruit luffa operculata fruit nasturtium officinale nasturtium officinale okoubaka aubrevillei bark okoubaka aubrevillei bark schoenocaulon officinale seed schoenocaulon officinale seed scrophularia nodosa scrophularia nodosa solidago virgaurea flowering top solidago virgaurea flowering top taraxacum officinale taraxacum officinale

Indications and Usage:

Uses: temporarily relieves coryza, cough and itchy eyes symptoms associated with hay fever and common allergens.** â**this statement has not been evaluated by the fda. it is based on documented homeopathic materia medica.

Warnings:

Warnings: keep out of the reach of children if pregnant or breast - feeding, ask a health professional before use. if symptons worsen or persist for more than a week, discontinue use and contact a doctor. do not use if cap seal is broken. keep out of the 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: use half the adults dose.

Package Label Principal Display Panel:

Homeopathic medicine ndc: 66096-710-05 allergy relief natural - safe - effective no side effects 2 fl oz (59 ml) / 15% alcohol 2oz bottle label natural - safe - effective no side effects

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.