NDC 79301-325 Alcohol Antiseptic 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:
79301-325
Proprietary Name:
Alcohol Antiseptic Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wenzhou Bangkang Biotechnology Co., Ltd
Labeler Code:
79301
Start Marketing Date: [9]
08-19-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 79301-325-01

Package Description: 4.5 g in 1 BOX

NDC Code 79301-325-02

Package Description: 45 g in 1 BOX

NDC Code 79301-325-03

Package Description: 135 g in 1 BOX

NDC Code 79301-325-04

Package Description: 225 g in 1 BOX

NDC Code 79301-325-05

Package Description: 360 g in 1 BOX

NDC Code 79301-325-06

Package Description: 352 g in 1 PAIL

Product Details

What is NDC 79301-325?

The NDC code 79301-325 is assigned by the FDA to the product Alcohol Antiseptic Wipes which is product labeled by Wenzhou Bangkang Biotechnology Co., Ltd. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 79301-325-01 4.5 g in 1 box , 79301-325-02 45 g in 1 box , 79301-325-03 135 g in 1 box , 79301-325-04 225 g in 1 box , 79301-325-05 360 g in 1 box , 79301-325-06 352 g in 1 pail . 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 Antiseptic Wipes?

Wipe the surface of the skin with a damp paper towel until it is dry. Do not rinse with water immediately after wiping.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Alcohol Antiseptic Wipes UNII Codes?

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

Which are Alcohol Antiseptic 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".