NDC 80404-301 Wipe Out Antibacterial Wipes Fresh Scent

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:
80404-301
Proprietary Name:
Wipe Out Antibacterial Wipes Fresh Scent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Xinsanyang Pharmaceutical (xiamen) Co., Ltd.
Labeler Code:
80404
Start Marketing Date: [9]
09-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 80404-301-01

Package Description: 1 CLOTH in 1 BAG

NDC Code 80404-301-02

Package Description: 10 CLOTH in 1 BAG

NDC Code 80404-301-03

Package Description: 20 CLOTH in 1 BAG

NDC Code 80404-301-04

Package Description: 40 CLOTH in 1 BAG

NDC Code 80404-301-05

Package Description: 60 CLOTH in 1 BAG

NDC Code 80404-301-06

Package Description: 80 CLOTH in 1 BAG

NDC Code 80404-301-07

Package Description: 100 CLOTH in 1 BAG

NDC Code 80404-301-08

Package Description: 120 CLOTH in 1 BAG

NDC Code 80404-301-09

Package Description: 200 CLOTH in 1 BAG

NDC Code 80404-301-10

Package Description: 400 CLOTH in 1 BAG

NDC Code 80404-301-11

Package Description: 500 CLOTH in 1 BAG

NDC Code 80404-301-12

Package Description: 600 CLOTH in 1 BAG

NDC Code 80404-301-13

Package Description: 800 CLOTH in 1 BAG

NDC Code 80404-301-14

Package Description: 1000 CLOTH in 1 BAG

Product Details

What is NDC 80404-301?

The NDC code 80404-301 is assigned by the FDA to the product Wipe Out Antibacterial Wipes Fresh Scent which is product labeled by Xinsanyang Pharmaceutical (xiamen) Co., Ltd.. The product's dosage form is . The product is distributed in 14 packages with assigned NDC codes 80404-301-01 1 cloth in 1 bag , 80404-301-02 10 cloth in 1 bag , 80404-301-03 20 cloth in 1 bag , 80404-301-04 40 cloth in 1 bag , 80404-301-05 60 cloth in 1 bag , 80404-301-06 80 cloth in 1 bag , 80404-301-07 100 cloth in 1 bag , 80404-301-08 120 cloth in 1 bag , 80404-301-09 200 cloth in 1 bag , 80404-301-10 400 cloth in 1 bag , 80404-301-11 500 cloth in 1 bag , 80404-301-12 600 cloth in 1 bag , 80404-301-13 800 cloth in 1 bag , 80404-301-14 1000 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 Wipe Out Antibacterial Wipes Fresh Scent?

WIPE OUT Antibacterial Wipes Fresh Scent to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Which are Wipe Out Antibacterial Wipes Fresh Scent UNII Codes?

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

Which are Wipe Out Antibacterial Wipes Fresh Scent 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 Wipe Out Antibacterial Wipes Fresh Scent?

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".