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  4. NDC Product Code: 71727-104 Puriface Spirulina Eye Gel Masks

NDC 71727-104 Puriface Spirulina Eye Gel Masks

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 71727-104?
  5. Puriface Spirulina Eye Gel Masks 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:
71727-104
Proprietary Name:
Puriface Spirulina Eye Gel Masks
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Imode Korea, Inc.
Labeler Code:
71727
Product Label ID:
8169d809-47a5-3f1e-e053-2991aa0a955c
Start Marketing Date: [9]
02-08-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 71727-104?

The NDC code 71727-104 is assigned by the FDA to the product Puriface Spirulina Eye Gel Masks which is product labeled by Imode Korea, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71727-104-02 1 pouch in 1 box / 27 ml in 1 pouch (71727-104-01). 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 Puriface Spirulina Eye Gel Masks?

Simply wash and dry your skin thoroughly. Before applying the gel under each eye, remove clear plastic from each gel. You may use either side of the gel. Allow gel to work for 15-20 minutes. Remove each gel and lightly massage any remaining serum into your skin.

Which are Puriface Spirulina Eye Gel Masks UNII Codes?

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

Which are Puriface Spirulina Eye Gel Masks 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".