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  4. NDC Product Code: 41546-011 Multi Surface Wipes 75% Alcohol

NDC 41546-011 Multi Surface Wipes 75% Alcohol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41546-011?
  4. Multi Surface Wipes 75% Alcohol 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:
41546-011
Proprietary Name:
Multi Surface Wipes 75% Alcohol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zhejiang Huanghua Biological Technology Co., Ltd
Labeler Code:
41546
Product Label ID:
b24d43de-df95-0503-e053-2995a90a7634
Start Marketing Date: [9]
10-23-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41546-011-01

Package Description: 80 CLOTH in 1 PAIL

Product Details

What is NDC 41546-011?

The NDC code 41546-011 is assigned by the FDA to the product Multi Surface Wipes 75% Alcohol which is product labeled by Zhejiang Huanghua Biological Technology Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41546-011-01 80 cloth 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 Multi Surface Wipes 75% Alcohol?

Wipe surface thoroughly

Which are Multi Surface Wipes 75% Alcohol UNII Codes?

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

Which are Multi Surface Wipes 75% Alcohol 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".