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  4. NDC Product Code: 55618-1001 Jilgyungyi

NDC 55618-1001 Jilgyungyi

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55618-1001?
  5. Jilgyungyi 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:
55618-1001
Proprietary Name:
Jilgyungyi
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ha U Dong Chun
Labeler Code:
55618
Product Label ID:
0579fcc7-e0c8-4958-8ab4-1ac8e8f7d88f
Start Marketing Date: [9]
06-11-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
OVAL (C48345)
Size(s):
12 MM
Imprint(s):
3;HP;X
Score:
1

Product Packages

NDC Code 55618-1001-1

Package Description: 20 TABLET in 1 PACKAGE

Product Details

What is NDC 55618-1001?

The NDC code 55618-1001 is assigned by the FDA to the product Jilgyungyi which is product labeled by Ha U Dong Chun. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55618-1001-1 20 tablet in 1 package . 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 Jilgyungyi?

This product is to be used in the vagina. Use it at bedtime, or during the day without dynamic activities. Insert the pills into your vagina with first two knuckles of your finger. During the 20 to 30 minutes the pills are melted and they are effective in improving vaginal health

Which are Jilgyungyi UNII Codes?

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

Which are Jilgyungyi 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:

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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".