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  4. NDC Product Code: 81855-001 Disinfecting Wet Wipes

NDC 81855-001 Disinfecting Wet Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81855-001?
  4. Disinfecting Wet Wipes 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:
81855-001
Proprietary Name:
Disinfecting Wet Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangsu Doublecotton Co.,ltd
Labeler Code:
81855
Product Label ID:
c0c681be-aa62-8dd3-e053-2995a90a7711
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81855-001?

The NDC code 81855-001 is assigned by the FDA to the product Disinfecting Wet Wipes which is product labeled by Jiangsu Doublecotton Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81855-001-01 40 cloth in 1 bag . 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 Disinfecting Wet Wipes?

Can be thrown directly into the toilet Can be used by the whole family Can be used during menstrual period Can be used by patients with hemorrhoids

Which are Disinfecting Wet Wipes UNII Codes?

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

Which are Disinfecting Wet Wipes 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".