NDC 80593-003 Antibacterial Wipes Unscented

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:
80593-003
Proprietary Name:
Antibacterial Wipes Unscented
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
80593
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 80593-003?

The NDC code 80593-003 is assigned by the FDA to the product Antibacterial Wipes Unscented which is product labeled by Zhangzhou Wansike Electronics Co., Ltd. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 80593-003-01 10 solution in 1 package , 80593-003-02 20 solution in 1 package , 80593-003-03 50 solution in 1 package , 80593-003-04 70 solution in 1 package , 80593-003-05 80 solution in 1 canister , 80593-003-06 100 solution in 1 canister , 80593-003-07 160 solution in 1 canister , 80593-003-08 300 solution in 1 canister , 80593-003-09 500 solution in 1 canister , 80593-003-10 800 solution in 1 canister . 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 Antibacterial Wipes Unscented?

Allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Which are Antibacterial Wipes Unscented UNII Codes?

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

Which are Antibacterial Wipes Unscented 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".