Band Leemyungnae Goyak

Elecampane Root, Forsythia Fruit

Chunwoo Pharmaceutical Co., Ltd.
Human Otc Drug
NDC 72850-0006

Band Leemyungnae Goyak also known as Elecampane Root, Forsythia Fruit is a human otc drug labeled by 'Chunwoo Pharmaceutical Co., Ltd.'. National Drug Code (NDC) number for Band Leemyungnae Goyak is 72850-0006. This drug is available in dosage form of Ointment. The names of the active, medicinal ingredients in Band Leemyungnae Goyak drug includes Atractylodes Lancea Root - 2 g/100g Chenopodium Album Whole - 52 g/100g Citrus Aurantium Fruit - 1 g/100g Forsythia Suspensa Fruit - 2 g/100g Frankincense - 1 g/100g Inula Helenium Root - 2 g/100g Lead Tetroxide - 33 g/100g Lonicera Dasystyla Flower Bud - 2 g/100g Morus Alba Stem - 2 g/100g Myrrh - 1 g/100g and more. The currest status of Band Leemyungnae Goyak drug is Active.

Drug Information:

Drug NDC:	72850-0006
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:	Band Leemyungnae Goyak
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:	Elecampane Root, Forsythia Fruit
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Chunwoo Pharmaceutical Co., Ltd.
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:	ATRACTYLODES LANCEA ROOT - 2 g/100g CHENOPODIUM ALBUM WHOLE - 52 g/100g CITRUS AURANTIUM FRUIT - 1 g/100g FORSYTHIA SUSPENSA FRUIT - 2 g/100g FRANKINCENSE - 1 g/100g INULA HELENIUM ROOT - 2 g/100g LEAD TETROXIDE - 33 g/100g LONICERA DASYSTYLA FLOWER BUD - 2 g/100g MORUS ALBA STEM - 2 g/100g MYRRH - 1 g/100g Load more... PRUNUS PERSICA LEAF - 2 g/100g PRUNUS PERSICA SEED - 1 g/100g PURSLANE - 3 g/100g SALIX ALBA BARK - 2 g/100g SULFUR - 1 g/100g
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 DRUG OTHER
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:	22 Mar, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	11 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:	Chunwoo Pharmaceutical Co., Ltd.
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:	CAZ6282J2O O417YBE692 DQD16J2B5O P4793M1ES5 R9XLF1R1WM E55SMD6DA8 A4G39L7HN2 J133K038DY 05Y42QCG2T JC71GJ1F3L Load more... VN3501T41P V9C81470RR M6S840WXG5 205MXS71H7 70FD1KFU70
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
72850-0006-1	3 g in 1 BOX (72850-0006-1)	22 Mar, 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

Band Leemyungnae Goyak

Elecampane Root, Forsythia Fruit

Ointment
Chunwoo Pharmaceutical Co., Ltd.
NDC: 72850-0006

Purpose:

â boil and pus remover. â help reducing the pain from a boil

Product Elements:

Band leemyungnae goyak elecampane root, forsythia fruit atractylodes lancea root atractylodes lancea root citrus aurantium fruit citrus aurantium fruit sucrose prunus persica leaf prunus persica leaf chenopodium album whole chenopodium album whole rice oil salix alba bark salix alba bark morus alba stem morus alba stem frankincense frankincense inula helenium root inula helenium root forsythia suspensa fruit forsythia suspensa fruit myrrh myrrh prunus persica seed prunus persica seed sulfur sulfur lonicera dasystyla flower bud lonicera dasystyla flower bud purslane purslane lead tetroxide lead tetroxide

Indications and Usage:

â wash your hands and clean affected area â before a boil or a pus is festering, attach the plaster only to cover the affected area. â when a boil or a pus festering, insert an uprooting ointment into the area and attach the plaster on it. â change to a new plaster after a day or two while symptom persists.

Warnings:

For external use only do not use if you are â under 7 â pregnant or breastfeeding â using around eyes ask a doctor before use â if you are allergic to any ingredients of this product. when using this product â avoid eating greasy food; pork, herring, mackerel, and etc. stop use and ask a doctor if you have â rash, itching or excessive skin irritation develops

Dosage and Administration:

For external use only

Package Label Principal Display Panel:

Label

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.