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  4. NDC Product Code: 72868-010 Medius Heart Ppyoung Ppyoung Eye

NDC 72868-010 Medius Heart Ppyoung Ppyoung Eye

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72868-010?
  4. Medius Heart Ppyoung Ppyoung Eye 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:
72868-010
Proprietary Name:
Medius Heart Ppyoung Ppyoung Eye
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aube. Corporation
Labeler Code:
72868
Product Label ID:
ee0684f4-0a73-4f7d-baab-58eefe71d910
Start Marketing Date: [9]
01-02-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 72868-010?

The NDC code 72868-010 is assigned by the FDA to the product Medius Heart Ppyoung Ppyoung Eye which is product labeled by Aube. Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72868-010-02 3 pouch in 1 carton / 5.5 g in 1 pouch (72868-010-01). 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 Medius Heart Ppyoung Ppyoung Eye?

Directions:1.After face wash, apply toner for basic care. 2.Take out the patch, remove films and tightly apply onto your face. 3.Enjoy your patch for about 30minutes so that the nutritious elements of the patch will get slowly absorbed. 4.Take off the patch, and get the leftover essence absorbed by lightly tapping your skin

Which are Medius Heart Ppyoung Ppyoung Eye UNII Codes?

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

Which are Medius Heart Ppyoung Ppyoung Eye 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".