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  4. NDC Product Code: 71609-0004 Moistie Pure Essence

NDC 71609-0004 Moistie Pure Essence

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71609-0004?
  4. Moistie Pure Essence Uses
  5. Active Ingredients UNII Codes
  6. 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:
71609-0004
Proprietary Name:
Moistie Pure Essence
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Purecell Korea Co., Ltd.
Labeler Code:
71609
Product Label ID:
562312c8-ce6d-5722-e054-00144ff88e88
Start Marketing Date: [9]
06-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71609-0004-1

Package Description: 3 VIAL in 1 PACKAGE / 10 mL in 1 VIAL

Product Details

What is NDC 71609-0004?

The NDC code 71609-0004 is assigned by the FDA to the product Moistie Pure Essence which is product labeled by Purecell Korea Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71609-0004-1 3 vial in 1 package / 10 ml in 1 vial. 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 Moistie Pure Essence?

Apply daily to your cleansed skin.Pure Essence can be attached to the Moistie Skin Therapy Steamer and used together with steam to make the skin clear and clean.

Which are Moistie Pure Essence UNII Codes?

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

Which are Moistie Pure Essence 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".