NDC 79293-001 Antibacterial 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:
79293-001
Proprietary Name:
Antibacterial Wet Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Fangyuan Textile Co., Ltd.
Labeler Code:
79293
Start Marketing Date: [9]
06-29-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 79293-001-01

Package Description: 200 BAG in 1 CARTON / 10 POUCH in 1 BAG / 48 g in 1 POUCH

NDC Code 79293-001-02

Package Description: 100 BAG in 1 CARTON / 15 POUCH in 1 BAG / 72 g in 1 POUCH

NDC Code 79293-001-03

Package Description: 100 BAG in 1 CARTON / 20 POUCH in 1 BAG / 96 g in 1 POUCH

NDC Code 79293-001-04

Package Description: 80 BAG in 1 CARTON / 25 POUCH in 1 BAG / 120 g in 1 POUCH

NDC Code 79293-001-05

Package Description: 60 BAG in 1 CARTON / 30 POUCH in 1 BAG / 144 g in 1 POUCH

NDC Code 79293-001-06

Package Description: 30 BAG in 1 CARTON / 50 POUCH in 1 BAG / 240 g in 1 POUCH

NDC Code 79293-001-07

Package Description: 30 BAG in 1 CARTON / 60 POUCH in 1 BAG / 288 g in 1 POUCH

NDC Code 79293-001-08

Package Description: 20 BAG in 1 CARTON / 80 POUCH in 1 BAG / 384 g in 1 POUCH

NDC Code 79293-001-09

Package Description: 12 BAG in 1 CARTON / 100 POUCH in 1 BAG / 480 g in 1 POUCH

NDC Code 79293-001-10

Package Description: 10 BAG in 1 CARTON / 120 POUCH in 1 BAG / 576 g in 1 POUCH

NDC Code 79293-001-11

Package Description: 200 BAG in 1 CARTON / 10 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-12

Package Description: 100 BAG in 1 CARTON / 15 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-13

Package Description: 100 BAG in 1 CARTON / 20 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-14

Package Description: 80 BAG in 1 CARTON / 25 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-15

Package Description: 60 BAG in 1 CARTON / 30 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-16

Package Description: 30 BAG in 1 CARTON / 50 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-17

Package Description: 30 BAG in 1 CARTON / 60 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-18

Package Description: 20 BAG in 1 CARTON / 80 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-19

Package Description: 12 BAG in 1 CARTON / 100 PATCH in 1 BAG / 4.8 g in 1 PATCH

NDC Code 79293-001-20

Package Description: 10 BAG in 1 CARTON / 120 PATCH in 1 BAG / 4.8 g in 1 PATCH

Product Details

What is NDC 79293-001?

The NDC code 79293-001 is assigned by the FDA to the product Antibacterial Wet Wipes which is product labeled by Hangzhou Fangyuan Textile Co., Ltd.. The product's dosage form is . The product is distributed in 20 packages with assigned NDC codes 79293-001-01 200 bag in 1 carton / 10 pouch in 1 bag / 48 g in 1 pouch, 79293-001-02 100 bag in 1 carton / 15 pouch in 1 bag / 72 g in 1 pouch, 79293-001-03 100 bag in 1 carton / 20 pouch in 1 bag / 96 g in 1 pouch, 79293-001-04 80 bag in 1 carton / 25 pouch in 1 bag / 120 g in 1 pouch, 79293-001-05 60 bag in 1 carton / 30 pouch in 1 bag / 144 g in 1 pouch, 79293-001-06 30 bag in 1 carton / 50 pouch in 1 bag / 240 g in 1 pouch, 79293-001-07 30 bag in 1 carton / 60 pouch in 1 bag / 288 g in 1 pouch, 79293-001-08 20 bag in 1 carton / 80 pouch in 1 bag / 384 g in 1 pouch, 79293-001-09 12 bag in 1 carton / 100 pouch in 1 bag / 480 g in 1 pouch, 79293-001-10 10 bag in 1 carton / 120 pouch in 1 bag / 576 g in 1 pouch, 79293-001-11 200 bag in 1 carton / 10 patch in 1 bag / 4.8 g in 1 patch, 79293-001-12 100 bag in 1 carton / 15 patch in 1 bag / 4.8 g in 1 patch, 79293-001-13 100 bag in 1 carton / 20 patch in 1 bag / 4.8 g in 1 patch, 79293-001-14 80 bag in 1 carton / 25 patch in 1 bag / 4.8 g in 1 patch, 79293-001-15 60 bag in 1 carton / 30 patch in 1 bag / 4.8 g in 1 patch, 79293-001-16 30 bag in 1 carton / 50 patch in 1 bag / 4.8 g in 1 patch, 79293-001-17 30 bag in 1 carton / 60 patch in 1 bag / 4.8 g in 1 patch, 79293-001-18 20 bag in 1 carton / 80 patch in 1 bag / 4.8 g in 1 patch, 79293-001-19 12 bag in 1 carton / 100 patch in 1 bag / 4.8 g in 1 patch, 79293-001-20 10 bag in 1 carton / 120 patch in 1 bag / 4.8 g in 1 patch. 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 Wet Wipes?

Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. Thoroughly wipe hands, allow to dry without rinsing. Discard after single use

Which are Antibacterial Wet Wipes UNII Codes?

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

Which are Antibacterial 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:

What is the NDC to RxNorm Crosswalk for Antibacterial Wet 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:

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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".