Dercut

Euphorbia Resinifera Resin, Goldenseal, Wood Creosote, Toxicodendron Pubescens Shoot, Sempervivum Tectorum Leaf, Bellis Perennis, Vinca Minor, And Viola Tricolor

Pekana Naturheilmittel Gmbh
Human Otc Drug
NDC 59469-307

Dercut also known as Euphorbia Resinifera Resin, Goldenseal, Wood Creosote, Toxicodendron Pubescens Shoot, Sempervivum Tectorum Leaf, Bellis Perennis, Vinca Minor, And Viola Tricolor is a human otc drug labeled by 'Pekana Naturheilmittel Gmbh'. National Drug Code (NDC) number for Dercut is 59469-307. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Dercut drug includes Bellis Perennis Whole - 8 [hp_X]/100g Euphorbia Resinifera Resin - 4 [hp_X]/100g Goldenseal - 4 [hp_X]/100g Pervinca Minor Whole - 3 [hp_X]/100g Sempervivum Tectorum Leaf - 3 [hp_X]/100g Toxicodendron Pubescens Shoot - 8 [hp_X]/100g Viola Tricolor Whole - 2 [hp_X]/100g Wood Creosote - 6 [hp_X]/100g . The currest status of Dercut drug is Active.

Drug Information:

Drug NDC:	59469-307
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:	Dercut
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:	Euphorbia Resinifera Resin, Goldenseal, Wood Creosote, Toxicodendron Pubescens Shoot, Sempervivum Tectorum Leaf, Bellis Perennis, Vinca Minor, And Viola Tricolor
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Pekana Naturheilmittel Gmbh
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:	BELLIS PERENNIS WHOLE - 8 [hp_X]/100g EUPHORBIA RESINIFERA RESIN - 4 [hp_X]/100g GOLDENSEAL - 4 [hp_X]/100g PERVINCA MINOR WHOLE - 3 [hp_X]/100g SEMPERVIVUM TECTORUM LEAF - 3 [hp_X]/100g TOXICODENDRON PUBESCENS SHOOT - 8 [hp_X]/100g VIOLA TRICOLOR WHOLE - 2 [hp_X]/100g WOOD CREOSOTE - 6 [hp_X]/100g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	CUTANEOUS
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, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	06 May, 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:	PEKANA Naturheilmittel GmbH
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.
UNII:	2HU33I03UY 1TI1O9028K ZW3Z11D0JV WGM46PQF02 3DGJ7BUA01 46PYZ1F82M 9Q24RAI43V 3JYG22FD73
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
59469-307-30	1 TUBE in 1 BOX (59469-307-30) / 30 g in 1 TUBE	24 Jun, 2019	N/A	No
59469-307-40	1 TUBE in 1 BOX (59469-307-40) / 100 g in 1 TUBE	24 Jun, 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

Dercut

Euphorbia Resinifera Resin & more..

Ointment
PEKANA Naturheilmittel GmbH
NDC: 59469-307

Purpose:

For relief of acne, eczema, itching, psoriasis, and skin irritation

Product Elements:

Dercut euphorbia resinifera resin, goldenseal, wood creosote, toxicodendron pubescens shoot, sempervivum tectorum leaf, bellis perennis, vinca minor, and viola tricolor euphorbia resinifera resin euphorbia resinifera resin goldenseal goldenseal wood creosote wood creosote toxicodendron pubescens shoot toxicodendron pubescens shoot sempervivum tectorum leaf sempervivum tectorum leaf bellis perennis whole bellis perennis whole pervinca minor whole pervinca minor whole viola tricolor whole viola tricolor whole medium-chain triglycerides cetostearyl alcohol cetyl alcohol spermaceti glycerin water alcohol

Indications and Usage:

Uses application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. these "uses" have not been evaluated by the food and drug administration. with severe forms of this disease, a clinically proven therapy is indicated. for relief of acne, eczema, itching, psoriasis, and skin irritation

Warnings:

Warnings for external use only. do not use on open wounds! if symptoms persist, contact a licensed practitioner. if you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. if you are pregnant or nursing a baby, seek the advice of a health care professional before use. keep out of the reach of children.

Dosage and Administration:

Directions unless otherwise prescribed, apply a moderate amount of ointment 2 to 3 times per day by rubbing gently into the affected area.

Package Label Principal Display Panel:

Principal display panel - 100 g tube box dercutâ¢ homeopathic ointment for relief of acne, eczema, itching, psoriasis, and skin irritation 3.5 oz 100 g pekana Â® principal display panel - 100 g tube box

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.