NDC 79294-001 Antiseptic Sanitizing 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:
79294-001
Proprietary Name:
Antiseptic Sanitizing Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Wipex Nonwovens Co., Ltd.
Labeler Code:
79294
Start Marketing Date: [9]
07-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 79294-001-01

Package Description: 160 BAG in 1 CARTON / 10 NOT APPLICABLE in 1 BAG / 60 g in 1 NOT APPLICABLE

NDC Code 79294-001-02

Package Description: 4 BAG in 1 CARTON / 1200 NOT APPLICABLE in 1 BAG / 4700 g in 1 NOT APPLICABLE

NDC Code 79294-001-03

Package Description: 48 BAG in 1 CARTON / 50 NOT APPLICABLE in 1 BAG / 237 g in 1 NOT APPLICABLE

NDC Code 79294-001-04

Package Description: 24 CANISTER in 1 CARTON / 80 NOT APPLICABLE in 1 CANISTER / 337 g in 1 NOT APPLICABLE

NDC Code 79294-001-05

Package Description: 24 CANISTER in 1 CARTON / 100 NOT APPLICABLE in 1 CANISTER / 540 g in 1 NOT APPLICABLE

NDC Code 79294-001-06

Package Description: 12 CANISTER in 1 CARTON / 180 NOT APPLICABLE in 1 CANISTER / 1120 g in 1 NOT APPLICABLE

NDC Code 79294-001-07

Package Description: 12 CANISTER in 1 CARTON / 220 NOT APPLICABLE in 1 CANISTER / 450 g in 1 NOT APPLICABLE

NDC Code 79294-001-08

Package Description: 4 BAG in 1 CARTON / 800 NOT APPLICABLE in 1 BAG / 1638 g in 1 NOT APPLICABLE

NDC Code 79294-001-09

Package Description: 4 BAG in 1 CARTON / 900 NOT APPLICABLE in 1 BAG / 1842 g in 1 NOT APPLICABLE

NDC Code 79294-001-10

Package Description: 4 BAG in 1 CARTON / 1500 NOT APPLICABLE in 1 BAG / 3071 g in 1 NOT APPLICABLE

Product Details

What is NDC 79294-001?

The NDC code 79294-001 is assigned by the FDA to the product Antiseptic Sanitizing Wipes which is product labeled by Hangzhou Wipex Nonwovens Co., Ltd.. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 79294-001-01 160 bag in 1 carton / 10 not applicable in 1 bag / 60 g in 1 not applicable, 79294-001-02 4 bag in 1 carton / 1200 not applicable in 1 bag / 4700 g in 1 not applicable, 79294-001-03 48 bag in 1 carton / 50 not applicable in 1 bag / 237 g in 1 not applicable, 79294-001-04 24 canister in 1 carton / 80 not applicable in 1 canister / 337 g in 1 not applicable, 79294-001-05 24 canister in 1 carton / 100 not applicable in 1 canister / 540 g in 1 not applicable, 79294-001-06 12 canister in 1 carton / 180 not applicable in 1 canister / 1120 g in 1 not applicable, 79294-001-07 12 canister in 1 carton / 220 not applicable in 1 canister / 450 g in 1 not applicable, 79294-001-08 4 bag in 1 carton / 800 not applicable in 1 bag / 1638 g in 1 not applicable, 79294-001-09 4 bag in 1 carton / 900 not applicable in 1 bag / 1842 g in 1 not applicable, 79294-001-10 4 bag in 1 carton / 1500 not applicable in 1 bag / 3071 g in 1 not applicable. 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 Antiseptic Sanitizing Wipes?

Wet hands thoroughly with product and allow to dry without wiping.

Which are Antiseptic Sanitizing Wipes UNII Codes?

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

Which are Antiseptic Sanitizing 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:

What is the NDC to RxNorm Crosswalk for Antiseptic Sanitizing Wipes?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

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".