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  4. NDC Product Code: 71224-0006 Quick Cleansing Dry Tissue

NDC 71224-0006 Quick Cleansing Dry Tissue

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71224-0006?
  4. Quick Cleansing Dry Tissue 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:
71224-0006
Proprietary Name:
Quick Cleansing Dry Tissue
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avajar Co Ltd
Labeler Code:
71224
Product Label ID:
627811f6-9265-61f0-e053-2991aa0af310
Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 71224-0006?

The NDC code 71224-0006 is assigned by the FDA to the product Quick Cleansing Dry Tissue which is product labeled by Avajar Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71224-0006-1 15 pouch in 1 package / 1 g in 1 pouch. 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 Quick Cleansing Dry Tissue?

1. Unfold the tissue and wet it slightly with water.2. Take the slightly wet tissue and do flexing motions to make the tissue foam.3. Softly wipe makeup away from the face.4. Rinse face with warm water.

Which are Quick Cleansing Dry Tissue UNII Codes?

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

Which are Quick Cleansing Dry Tissue 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".