NDC 80515-002 99.99% Disinfection Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80515-002
Proprietary Name:
99.99% Disinfection Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
80515
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 80515-002?

The NDC code 80515-002 is assigned by the FDA to the product 99.99% Disinfection Wipes which is product labeled by Quanzhou V-care Sanitary Products Co.,ltd. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 80515-002-01 10 cloth in 1 bag , 80515-002-02 20 cloth in 1 bag , 80515-002-03 40 cloth in 1 bag , 80515-002-04 50 cloth in 1 bag , 80515-002-05 60 cloth in 1 bag , 80515-002-06 80 cloth in 1 bag , 80515-002-07 100 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 99.99% Disinfection Wipes?

Gently open the protective seal Remove the wipes from the package and use it directly on the skin Use the wipe to clean and avoid to use on sensitive areas, such as eyes and wounds Once you have finished, close the package by pressing the protactive seal Avoid to keep the protective seal uncovered

Which are 99.99% Disinfection Wipes UNII Codes?

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

Which are 99.99% Disinfection 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".