NDC 79758-001 75% Alcohol Wet 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:
79758-001
Proprietary Name:
75% Alcohol Wet Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
79758
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 79758-001?

The NDC code 79758-001 is assigned by the FDA to the product 75% Alcohol Wet Wipes which is product labeled by Lechang Baochuang Environmental Protection New Materials Co.,ltd.. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 79758-001-01 1 cloth in 1 bag , 79758-001-02 8 cloth in 1 bag , 79758-001-03 10 cloth in 1 bag , 79758-001-04 20 cloth in 1 bag , 79758-001-05 25 cloth in 1 bag , 79758-001-06 30 cloth in 1 bag , 79758-001-07 50 cloth in 1 bag , 79758-001-08 80 cloth in 1 bag , 79758-001-09 100 cloth in 1 bag , 79758-001-10 120 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 75% Alcohol Wet Wipes?

1. When using, please open the sealing cover on the package; 2. Take out a wet towel from the paper outlet; 3. After use, the sealing cover should be covered to prevent the wet towel from drying. 4.Get a wet wipe to scrub skin and daily using, supervise children under 6 years of age when using this product to avoid swallowing.

Which are 75% Alcohol Wet Wipes UNII Codes?

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

Which are 75% Alcohol 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".