Eye Strain Relief Pm

Conium Maculatum, Euphrasia, Natrium Muriaticum, Physostigma Venenosum, Ruta Graveolens, Senega Officinalis, Valeriana Officinalis

Trp Company
Human Otc Drug
NDC 17312-174

Eye Strain Relief Pm also known as Conium Maculatum, Euphrasia, Natrium Muriaticum, Physostigma Venenosum, Ruta Graveolens, Senega Officinalis, Valeriana Officinalis is a human otc drug labeled by 'Trp Company'. National Drug Code (NDC) number for Eye Strain Relief Pm is 17312-174. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Eye Strain Relief Pm drug includes Conium Maculatum Flowering Top - 6 [hp_X]/4g Euphrasia Stricta - 6 [hp_X]/4g Physostigma Venenosum Seed - 13 [hp_X]/4g Polygala Senega Root - 6 [hp_X]/4g Ruta Graveolens Flowering Top - 6 [hp_X]/4g Sodium Chloride - 8 [hp_X]/4g Valerian - 6 [hp_X]/4g . The currest status of Eye Strain Relief Pm drug is Active.

Drug Information:

Drug NDC:	17312-174
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:	Eye Strain Relief Pm
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:	Conium Maculatum, Euphrasia, Natrium Muriaticum, Physostigma Venenosum, Ruta Graveolens, Senega Officinalis, Valeriana Officinalis
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Trp Company
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Ointment
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:	CONIUM MACULATUM FLOWERING TOP - 6 [hp_X]/4g EUPHRASIA STRICTA - 6 [hp_X]/4g PHYSOSTIGMA VENENOSUM SEED - 13 [hp_X]/4g POLYGALA SENEGA ROOT - 6 [hp_X]/4g RUTA GRAVEOLENS FLOWERING TOP - 6 [hp_X]/4g SODIUM CHLORIDE - 8 [hp_X]/4g VALERIAN - 6 [hp_X]/4g
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:	15 Apr, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	23 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, 2024
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:	TRP Company
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:	0858961001747
UPC stands for Universal Product Code.
UNII:	Q28R5GF371 C9642I91WL CJV9E9IIOA M7T6H7D4IF N94C2U587S 451W47IQ8X JWF5YAW3QW
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
17312-174-13	1 TUBE in 1 PACKAGE (17312-174-13) / 4 g in 1 TUBE	15 Apr, 2019	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

Eye Strain Relief Pm

Conium Maculatum & more..

Ointment
TRP Company
NDC: 17312-174

Purpose:

Conium maculatum - eye fatigue, drooping lids euphrasia - dryness, redness natrium muriaticum - difficulty reading physostigma venenosum - myopia, difficulty focusing ruta graveolens - eye strain with headaches, tired eyes senega officinalis - double vision valeriana officinalis - sleeplessness

Product Elements:

Eye strain relief pm conium maculatum, euphrasia, natrium muriaticum, physostigma venenosum, ruta graveolens, senega officinalis, valeriana officinalis valerian valerian lactose lanolin alcohols mineral oil petrolatum physostigma venenosum seed physostigma venenosum seed sodium chloride chloride ion euphrasia stricta euphrasia stricta conium maculatum flowering top conium maculatum flowering top ruta graveolens flowering top ruta graveolens flowering top polygala senega root polygala senega root

Indications and Usage:

Uses* â¢ according to homeopathic indications these ingredients provide temporary relief from symptoms such as: â¢ dry, red, tired eyes â¢ eye strain â¢headache â¢ double vision â¢ difficulty focusing â¢ difficulty reading â¢ eye fatigue â¢ irritated eyes â¢ sleeplessness; after serious causes have been ruled out by a physician. *these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.

Warnings:

Warnings: a physician should always be consulted to rule out serious causes. for external use only. this product is intended to complement, not replace, standard medical treatment. initial worsening of symptoms may occur.

Replace cap after every use. to avoid contamination - do not touch tip to any surface. use within 30 days of opening, expiration date only refers to the unopened tube. contact lens wearers: consult a physician before use.

Do Not Use:

Dosage and Administration:

Directions: suitable for adults and children ages 2 and over. children under the age of 2: consult a physician before use. wash your hands. before bedtime, pull down the lower lid of the affected eye and apply a small 1/4 inch of ointment, to the inside of the eyelid. close the eye to allow contact with the eye. homeopathic remedies may not be effective for everyone. individual results may vary.

Stop Use:

Stop use and ask a doctor if: you experience eye pain, changes in vision, continued redness or irritation of the eye. the condition worsens. the condition last longer than 72 hours.

Package Label Principal Display Panel:

Do not use if tamper evident carton seals are torn, broken or missing. fda disclaimer: claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated. carton label

Further Questions:

Questions or comments? call: 888-969-6855

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.