NDC 54141-002 Nsure Kleenwipe Sanitizing Wet Wipes

Benzalkonium Chloride

NDC Product Code 54141-002

NDC CODE: 54141-002

Proprietary Name: Nsure Kleenwipe Sanitizing Wet Wipes What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Benzalkonium Chloride What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 54141 - Fuzhou Juanjuan Non-woven Products Co., Ltd.
    • 54141-002 - Nsure Kleenwipe Sanitizing Wet Wipes

NDC 54141-002-01

Package Description: 160 PACKAGE in 1 CANISTER > 5.57 mL in 1 PACKAGE

NDC Product Information

Nsure Kleenwipe Sanitizing Wet Wipes with NDC 54141-002 is a a human over the counter drug product labeled by Fuzhou Juanjuan Non-woven Products Co., Ltd.. The generic name of Nsure Kleenwipe Sanitizing Wet Wipes is benzalkonium chloride. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Fuzhou Juanjuan Non-woven Products Co., Ltd.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Nsure Kleenwipe Sanitizing Wet Wipes Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BENZALKONIUM CHLORIDE .1 g/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • BIGUANIDE (UNII: FB4Q52I9K2)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Fuzhou Juanjuan Non-woven Products Co., Ltd.
Labeler Code: 54141
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 01-30-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Nsure Kleenwipe Sanitizing Wet Wipes Product Label Images

Nsure Kleenwipe Sanitizing Wet Wipes Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Indications And Usage

• For hand washing to decrease bacteria on the skin.  Recommended for repeat use.

Warnings

  • For external use only.Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.Do not use if you are allergic to any of the ingredients.Discontinue use if irritation or redness develops,and if condition persists for more than 72 hours consult a physician.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children unless under adult supervisionIf swallowed, get medical help.

Directions Of Use

  • Wet hands thoroughly with product and allow to dry without rinse.Children under six years of age should be supervised when using this product.

Other Information

  • Store in a dry place away from fire.

Inactive Ingredients

  • Glycerin, Propylene Glycol, Water, Biguanide

* Please review the disclaimer below.