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  4. NDC Product Code: 90028-060 Prepiel K365 Clean Tissue

NDC 90028-060 Prepiel K365 Clean Tissue

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 90028-060?
  4. Prepiel K365 Clean 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:
90028-060
Proprietary Name:
Prepiel K365 Clean Tissue
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jmb Cosline Co.,ltd
Labeler Code:
90028
Product Label ID:
bae8800c-f8d4-1ada-e053-2995a90ae8af
Start Marketing Date: [9]
02-09-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 90028-060?

The NDC code 90028-060 is assigned by the FDA to the product Prepiel K365 Clean Tissue which is product labeled by Jmb Cosline Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 90028-060-01 20 cloth in 1 packet . 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 Prepiel K365 Clean Tissue?

■ Use one or several sheets to rub well and dry.■ Supervise children under 6 years of age when using this product to avoid swallowing. ■ Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.)■ This product is intended only for hand sanitizing. ■ To prevent contents from drying out and contaminants from entering, close lid completely after use. ■ Keep product in its original container as storing the product in anything other than the original container may result in accidents or cause the integrity of the product to diminish. ■ Do not use over bandages, castings, etc. as irritation may occur.

Which are Prepiel K365 Clean Tissue UNII Codes?

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

Which are Prepiel K365 Clean 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".