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  4. NDC Product Code: 50300-010 Goong Mahn Geum

NDC 50300-010 Goong Mahn Geum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50300-010?
  5. Goong Mahn Geum Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50300-010
Proprietary Name:
Goong Mahn Geum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chung Sol
Labeler Code:
50300
Product Label ID:
9bc9795a-5d34-4512-bfb4-26e15fa0ae13
Start Marketing Date: [9]
03-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLACK (C48323)
Shape:
ROUND (C48348)
Size(s):
15 MM
Imprint(s):
GOONG
Score:
1

Product Packages

NDC Code 50300-010-01

Package Description: 12 PILL in 1 CARTON

Product Details

What is NDC 50300-010?

The NDC code 50300-010 is assigned by the FDA to the product Goong Mahn Geum which is product labeled by Chung Sol. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50300-010-01 12 pill in 1 carton . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Goong Mahn Geum?

Indication and usage:1. Insert to the vagina when you sleep before2. 2days later pull the thread3. take a sitz bath with warm water and discharge waste from the body4. wear your pad

Which are Goong Mahn Geum UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Goong Mahn Geum Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".