NDC 81551-000 Noble Chemical Free And Clear Liquid E2 Sanitizing Hand

Benzalkonium Chloride

NDC Product Code 81551-000

NDC CODE: 81551-000

Proprietary Name: Noble Chemical Free And Clear Liquid E2 Sanitizing Hand 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

  • 81551 - Noble Chemical
    • 81551-000 - Noble Chemical Free And Clear Liquid E2 Sanitizing Hand

NDC 81551-000-00

Package Description: 3785 mL in 1 BOTTLE

NDC Product Information

Noble Chemical Free And Clear Liquid E2 Sanitizing Hand with NDC 81551-000 is a a human over the counter drug product labeled by Noble Chemical. The generic name of Noble Chemical Free And Clear Liquid E2 Sanitizing Hand is benzalkonium chloride. The product's dosage form is liquid and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1046593.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Noble Chemical Free And Clear Liquid E2 Sanitizing Hand 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.


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.

  • WATER (UNII: 059QF0KO0R)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)

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: Noble Chemical
Labeler Code: 81551
FDA Application Number: part333E 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: 07-01-2021 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 - NO 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".

* Please review the disclaimer below.

Noble Chemical Free And Clear Liquid E2 Sanitizing Hand Product Label Images

Noble Chemical Free And Clear Liquid E2 Sanitizing Hand 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 Ingredient

Benzalkonium Chloride 0.13% w/v

Purpose

Antibacterial Agent

Uses

For handwashing to decrease bacteria on skin.

Warnings

For external use only.

Do Not Use

In the eyes. If eye contact occurs, flush with water.

Stop Use And Ask A Doctor If

Redness and irritation occur and last for more than 72 hours.

Keep Out Of Reach Of Children.

If swallowed, contact a physician or poison control center.

Directions

Apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

Inactive Ingredients

Water, Ammonium Lauryl Ether Sulfate, Cocamidopropyl Betaine, Sodium Dodecylbenzene Sulfonate, Salt

* Please review the disclaimer below.