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  4. NDC Product Code: 69351-020 Soosul Ginseng

NDC 69351-020 Soosul Ginseng

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69351-020?
  4. Soosul Ginseng Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69351-020
Proprietary Name:
Soosul Ginseng
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sang Hwang Mi-in Co., Ltd.
Labeler Code:
69351
Product Label ID:
214330a1-7e20-42fc-a885-d49bc181f20b
Start Marketing Date: [9]
10-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69351-020-01

Package Description: 60 g in 1 CARTON

Product Details

What is NDC 69351-020?

The NDC code 69351-020 is assigned by the FDA to the product Soosul Ginseng which is product labeled by Sang Hwang Mi-in Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69351-020-01 60 g 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 Soosul Ginseng?

Indications:Contains 15% of highly concentrated Sang-hwang mushroom extract, Korean Ginseng and various natural medicinal herbs, this nutrient-rich luxurious cream moisturizes, nourishes and calms your skin from within. It helps to erase the freckle, smoothen fine lines and revitalize youthfulness, promoting healthy looking skin and leaving it soft and supple.

Which are Soosul Ginseng UNII Codes?

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

Which are Soosul Ginseng 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:

What is the NDC to RxNorm Crosswalk for Soosul Ginseng?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".