NDC 79795-003 Alcohol Wipes (75% Alcohol)

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:
Proprietary Name:
Alcohol Wipes (75% Alcohol)
Product Type: [3]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79795-003?

The NDC code 79795-003 is assigned by the FDA to the product Alcohol Wipes (75% Alcohol) which is product labeled by Nantong Guarder Medical Technology Co.,ltd.. The product's dosage form is . The product is distributed in 16 packages with assigned NDC codes 79795-003-01 3 cloth in 1 bag , 79795-003-02 5 cloth in 1 bag , 79795-003-03 10 cloth in 1 bag , 79795-003-04 20 cloth in 1 bag , 79795-003-05 50 cloth in 1 bag , 79795-003-06 80 cloth in 1 bag , 79795-003-07 75 cloth in 1 box , 79795-003-08 80 cloth in 1 box , 79795-003-09 100 cloth in 1 box , 79795-003-10 150 cloth in 1 box , 79795-003-11 160 cloth in 1 box , 79795-003-12 200 cloth in 1 box , 79795-003-13 600 cloth in 1 box , 79795-003-14 800 cloth in 1 box , 79795-003-15 1000 cloth in 1 box , 79795-003-16 1200 cloth in 1 box . 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 Alcohol Wipes (75% Alcohol)?

Wet hands thoroughly with product and allow to dry.Dicard wipes in trash receptacle after use. Do not flush.Children under 6 years of age should be supervised when using this product.

Which are Alcohol Wipes (75% Alcohol) UNII Codes?

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

Which are Alcohol Wipes (75% Alcohol) 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".