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  4. NDC Product Code: 80707-201 Disinfecting Wipes

NDC 80707-201 Disinfecting Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80707-201?
  4. Disinfecting Wipes Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80707-201
Proprietary Name:
Disinfecting Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Muzi Commodity Co., Ltd
Labeler Code:
80707
Product Label ID:
b6a4c470-3ced-1aff-e053-2995a90a509c
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80707-201-01

Package Description: 35 CLOTH in 1 BOTTLE

NDC Code 80707-201-02

Package Description: 40 CLOTH in 1 BOTTLE

NDC Code 80707-201-03

Package Description: 50 CLOTH in 1 BOTTLE

NDC Code 80707-201-04

Package Description: 60 CLOTH in 1 BOTTLE

NDC Code 80707-201-05

Package Description: 70 CLOTH in 1 BOTTLE

NDC Code 80707-201-06

Package Description: 75 CLOTH in 1 BOTTLE

NDC Code 80707-201-07

Package Description: 80 CLOTH in 1 BOTTLE

NDC Code 80707-201-08

Package Description: 90 CLOTH in 1 BOTTLE

NDC Code 80707-201-09

Package Description: 100 CLOTH in 1 BOTTLE

NDC Code 80707-201-10

Package Description: 120 CLOTH in 1 BOTTLE

NDC Code 80707-201-11

Package Description: 150 CLOTH in 1 BOTTLE

NDC Code 80707-201-12

Package Description: 160 CLOTH in 1 BOTTLE

NDC Code 80707-201-13

Package Description: 180 CLOTH in 1 BOTTLE

NDC Code 80707-201-14

Package Description: 200 CLOTH in 1 BOTTLE

NDC Code 80707-201-15

Package Description: 250 CLOTH in 1 BOTTLE

NDC Code 80707-201-16

Package Description: 300 CLOTH in 1 BOTTLE

Product Details

What is NDC 80707-201?

The NDC code 80707-201 is assigned by the FDA to the product Disinfecting Wipes which is product labeled by Hangzhou Muzi Commodity Co., Ltd. The product's dosage form is . The product is distributed in 16 packages with assigned NDC codes 80707-201-01 35 cloth in 1 bottle , 80707-201-02 40 cloth in 1 bottle , 80707-201-03 50 cloth in 1 bottle , 80707-201-04 60 cloth in 1 bottle , 80707-201-05 70 cloth in 1 bottle , 80707-201-06 75 cloth in 1 bottle , 80707-201-07 80 cloth in 1 bottle , 80707-201-08 90 cloth in 1 bottle , 80707-201-09 100 cloth in 1 bottle , 80707-201-10 120 cloth in 1 bottle , 80707-201-11 150 cloth in 1 bottle , 80707-201-12 160 cloth in 1 bottle , 80707-201-13 180 cloth in 1 bottle , 80707-201-14 200 cloth in 1 bottle , 80707-201-15 250 cloth in 1 bottle , 80707-201-16 300 cloth in 1 bottle . 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 Disinfecting Wipes?

Wet hands thoroghly with product and allow to dry.Discard wipes in trash receptacle after use. Do not flush.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Disinfecting Wipes UNII Codes?

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

Which are Disinfecting 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".