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  4. NDC Product Code: 79953-750 Alcohol Wipes

NDC 79953-750 Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 79953-750?
  5. Alcohol Wipes Uses
  6. Active Ingredients UNII Codes
  7. 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:
79953-750
Proprietary Name:
Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Protective Suppliers Llc
Labeler Code:
79953
Product Label ID:
ac38df88-ac94-92e4-e053-2995a90a4165
Start Marketing Date: [9]
08-06-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 79953-750-01

Package Description: 750 PATCH in 1 PACKAGE / 4.67 g in 1 PATCH

Product Details

What is NDC 79953-750?

The NDC code 79953-750 is assigned by the FDA to the product Alcohol Wipes which is product labeled by Protective Suppliers Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79953-750-01 750 patch in 1 package / 4.67 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 Alcohol Wipes?

Remove top, remove foil,lift pop top,feed wipe through opening, and gently pull to remove wipe. Gently wipe hands to remove germs and becteria. After use, close top to keep wipes moist. Do not flush, please discard wipe in trash after use. Please recycle canister where possible.

Which are Alcohol Wipes UNII Codes?

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

Which are Alcohol 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:

* 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".