Ohm Allergy Mold Mix

Alternaria Alt, Aspergillus Fum, Aspergillus Nig, Boletus Sat, Botrytis Cin, Candida Alb, Cladosporium Met, Fusarium Oxy, Helminthosporium, Murcor Mue, Pullularia Pul, Rhizopus Nig, Ustaligo, Histaminum.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-670

Ohm Allergy Mold Mix also known as Alternaria Alt, Aspergillus Fum, Aspergillus Nig, Boletus Sat, Botrytis Cin, Candida Alb, Cladosporium Met, Fusarium Oxy, Helminthosporium, Murcor Mue, Pullularia Pul, Rhizopus Nig, Ustaligo, Histaminum. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Allergy Mold Mix is 66096-670. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Ohm Allergy Mold Mix drug includes Alternaria Alternata - 14 [hp_X]/59mL Aspergillus Fumigatus - 14 [hp_X]/59mL Aspergillus Niger Var. Niger - 14 [hp_X]/59mL Aureobasidium Pullulans Var. Pullutans - 14 [hp_X]/59mL Boletus Satanas Fruiting Body - 14 [hp_X]/59mL Botrytis Cinerea - 14 [hp_X]/59mL Candida Albicans - 14 [hp_X]/59mL Cochliobolus Sativus - 14 [hp_X]/59mL Fusarium Oxysporum - 14 [hp_X]/59mL Histamine Dihydrochloride - 60 [hp_X]/59mL and more. The currest status of Ohm Allergy Mold Mix drug is Active.

Drug Information:

Drug NDC:	66096-670
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 Allergy Mold Mix
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:	Alternaria Alt, Aspergillus Fum, Aspergillus Nig, Boletus Sat, Botrytis Cin, Candida Alb, Cladosporium Met, Fusarium Oxy, Helminthosporium, Murcor Mue, Pullularia Pul, Rhizopus Nig, Ustaligo, Histaminum.
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:	ALTERNARIA ALTERNATA - 14 [hp_X]/59mL ASPERGILLUS FUMIGATUS - 14 [hp_X]/59mL ASPERGILLUS NIGER VAR. NIGER - 14 [hp_X]/59mL AUREOBASIDIUM PULLULANS VAR. PULLUTANS - 14 [hp_X]/59mL BOLETUS SATANAS FRUITING BODY - 14 [hp_X]/59mL BOTRYTIS CINEREA - 14 [hp_X]/59mL CANDIDA ALBICANS - 14 [hp_X]/59mL COCHLIOBOLUS SATIVUS - 14 [hp_X]/59mL FUSARIUM OXYSPORUM - 14 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE - 60 [hp_X]/59mL Load more... PASSALORA FULVA - 14 [hp_X]/59mL RHIZOPUS STOLONIFER - 14 [hp_X]/59mL USTILAGO MAYDIS - 14 [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:	29 Oct, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	18 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:	0366096670054
UPC stands for Universal Product Code.
NUI:	N0000185372 N0000175629 N0000184306 N0000185001 M0008890 M0000728
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	52B29REC7H X88DF51T48 9IOA40ANG6 D1A2NG69CK 68OG1407SM TBW53313S7 4D7G21HDBC 3LN5B70U4W 5398RXP8KU 3POA0Q644U Load more... HR6H5057CO FEE198DK4Q 4K7Z7K7SWG
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:	Non-Standardized Fungal 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:	Fungal Proteins [CS] Allergens [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] Cell-mediated Immunity [PE] Fungal Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Non-Standardized Fungal Allergenic Extract [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
66096-670-05	59 mL in 1 PACKAGE (66096-670-05)	29 Oct, 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 Allergy Mold Mix

Alternaria Alt & more..

Liquid
OHM PHARMA INC.
NDC: 66096-670

Purpose:

Temporarily relieves sneezing, runny nose, itchy eyes, associated with exposure to molds and fungi.**

Product Elements:

Ohm allergy mold mix alternaria alt, aspergillus fum, aspergillus nig, boletus sat, botrytis cin, candida alb, cladosporium met, fusarium oxy, helminthosporium, murcor mue, pullularia pul, rhizopus nig, ustaligo, histaminum. alcohol glycerin water alternaria alternata alternaria alternata aspergillus fumigatus aspergillus fumigatus aspergillus niger var. niger aspergillus niger var. niger boletus satanas fruiting body boletus satanas fruiting body botrytis cinerea botrytis cinerea candida albicans candida albicans passalora fulva passalora fulva fusarium oxysporum fusarium oxysporum cochliobolus sativus cochliobolus sativus aureobasidium pullulans var. pullutans aureobasidium pullulans var. pullutans rhizopus stolonifer rhizopus stolonifer ustilago maydis ustilago maydis histamine dihydrochloride histamine

Indications and Usage:

Uses: temporarily relieves sneezing, runny nose, itchy eyes associated with exposure to molds and fungi.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

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 & 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: 66096-670-05 allergy mold mix natural - safe - effective no side effects 2 fl oz (59 ml) / 15% alcohol image description temporarily relieves sneezing, runny nose, itchy eyes, associated with exposure to molds and fungi.**

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.