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  4. NDC Product Code: 72058-030 Do Good Perfecting Aqua Mask 5ea

NDC 72058-030 Do Good Perfecting Aqua Mask 5ea

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72058-030?
  4. Do Good Perfecting Aqua Mask 5ea 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:
72058-030
Proprietary Name:
Do Good Perfecting Aqua Mask 5ea
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wooree Colourone Co.,ltd
Labeler Code:
72058
Product Label ID:
64491c83-ae5d-44cc-942e-3ec7e89771d7
Start Marketing Date: [9]
01-02-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72058-030-02

Package Description: 5 POUCH in 1 CARTON / 25 g in 1 POUCH (72058-030-01)

Product Details

What is NDC 72058-030?

The NDC code 72058-030 is assigned by the FDA to the product Do Good Perfecting Aqua Mask 5ea which is product labeled by Wooree Colourone Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72058-030-02 5 pouch in 1 carton / 25 g in 1 pouch (72058-030-01). 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 Do Good Perfecting Aqua Mask 5ea?

Directions: 1. Cleanse your face thoroughly 2. Open the pouch and evenly spread the mask on your face. 3. Leave on your face for 10~20 minutes. 4. Remove the mask gently and pat remaining essence to fully absorb

Which are Do Good Perfecting Aqua Mask 5ea UNII Codes?

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

Which are Do Good Perfecting Aqua Mask 5ea 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".