Ohm Venous Aid

Aesculus Hippocastanum, Arnica Montana, Calendula Officinalis, Echinacea Purpurea, Hamamelis Virginiana, Paeonia Officinalis, Ratanhia.

Ohm Pharma Inc.
Human Prescription Drug
NDC 66096-341

Ohm Venous Aid also known as Aesculus Hippocastanum, Arnica Montana, Calendula Officinalis, Echinacea Purpurea, Hamamelis Virginiana, Paeonia Officinalis, Ratanhia. is a human prescription drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Venous Aid is 66096-341. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Ohm Venous Aid drug includes Arnica Montana - 1 [hp_X]/96.5g Calendula Officinalis Flowering Top - 1 [hp_X]/96.5g Echinacea Purpurea - 1 [hp_X]/96.5g Hamamelis Virginiana Root Bark/stem Bark - 3 [hp_X]/96.5g Horse Chestnut - 1 [hp_X]/96.5g Krameria Lappacea Root - 3 [hp_X]/96.5g Paeonia Officinalis Root - 1 [hp_X]/96.5g . The currest status of Ohm Venous Aid drug is Active.

Drug Information:

Drug NDC:	66096-341
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 Venous Aid
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Prescription 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:	Aesculus Hippocastanum, Arnica Montana, Calendula Officinalis, Echinacea Purpurea, Hamamelis Virginiana, Paeonia Officinalis, Ratanhia.
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:	Cream
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:	ARNICA MONTANA - 1 [hp_X]/96.5g CALENDULA OFFICINALIS FLOWERING TOP - 1 [hp_X]/96.5g ECHINACEA PURPUREA - 1 [hp_X]/96.5g HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - 3 [hp_X]/96.5g HORSE CHESTNUT - 1 [hp_X]/96.5g KRAMERIA LAPPACEA ROOT - 3 [hp_X]/96.5g PAEONIA OFFICINALIS ROOT - 1 [hp_X]/96.5g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	TOPICAL
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:	24 Jun, 2015
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	13 Jan, 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:	0366096341107
UPC stands for Universal Product Code.
UNII:	O80TY208ZW 18E7415PXQ QI7G114Y98 T7S323PKJS 3C18L6RJAZ P29ZH1A35Z 8R564U2E1P
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
66096-341-10	96.5 g in 1 BOTTLE, PUMP (66096-341-10)	24 Jun, 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 Venous Aid

Aesculus Hippocastanum & more..

Cream
OHM PHARMA INC.
NDC: 66096-341

Purpose:

Relieves minor pain.

Product Elements:

Ohm venous aid aesculus hippocastanum, arnica montana, calendula officinalis, echinacea purpurea, hamamelis virginiana, paeonia officinalis, ratanhia. sodium borate caprylyl glycol polysorbate 60 lavender oil aloe vera leaf coconut oil sunflower oil phenoxyethanol water .alpha.-tocopherol horse chestnut horse chestnut arnica montana arnica montana calendula officinalis flowering top calendula officinalis flowering top echinacea purpurea echinacea purpurea hamamelis virginiana root bark/stem bark hamamelis virginiana root bark/stem bark paeonia officinalis root paeonia officinalis root krameria lappacea root krameria lappacea root

Indications and Usage:

Uses: temporarily relieves minor pain and discomfort due to varicose veins, improving blood vessels tone and relieving inflammation. also effective in the hemorrhoidal plexus.** â**this statement has not been evaluated by the fda. it is based on documented homeopathic materia medica.

Warnings:

Warning: for topical use only. do not apply to broken skin. if pregnant or breast-feeding, ask a health professional before use. if symptoms worsen or persist for more than one week, discontinue use and contact a health care professional. in case of overdose (or accidental ingestion) get medical help or contact a poison control center right away. âkeep out of reach of children.

Dosage and Administration:

Directions: apply a small amount to affected area 3 times a day or as directed by a health care professional.

Package Label Principal Display Panel:

Ndc: 66096-341-10 ohm venous aid cream natural - safe - effective no side effects topical homeopathic net wt: 3.40oz (96.5g) made in usa 3.40oz bottle label relieves minor pain.

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.