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  4. NDC Product Code: 81593-0001 My One-day Mask

NDC 81593-0001 My One-day Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81593-0001?
  4. My One-day Mask 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:
81593-0001
Proprietary Name:
My One-day Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Taechang Ever Green Co Ltd
Labeler Code:
81593
Product Label ID:
bc6f2d4a-2d8b-510e-e053-2995a90af163
Start Marketing Date: [9]
03-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81593-0001-1

Package Description: 3 g in 1 PACKAGE

Product Details

What is NDC 81593-0001?

The NDC code 81593-0001 is assigned by the FDA to the product My One-day Mask which is product labeled by Taechang Ever Green Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81593-0001-1 3 g in 1 package . 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 My One-day Mask?

Place the mask on your face to cover your nose and chin

Which are My One-day Mask UNII Codes?

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

  • POLYPROPYLENE (30000 MW) (UNII: T71QXI2O62)
  • POLYPROPYLENE (30000 MW) (UNII: T71QXI2O62) (Active Moiety)

Which are My One-day Mask 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".