NDC 11084-702 Appeal Alcohol Foaming Hand Sanitizer
Ethyl Alcohol Liquid Topical

Product Information

What is NDC 11084-702?

The NDC code 11084-702 is assigned by the FDA to the product Appeal Alcohol Foaming Hand Sanitizer which is a human over the counter drug product labeled by Sc Johnson Professional Usa, Inc.. The generic name of Appeal Alcohol Foaming Hand Sanitizer is ethyl alcohol. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 11084-702-27 1000 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code11084-702
Proprietary Name 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.		Appeal Alcohol Foaming Hand Sanitizer
Non-Proprietary Name 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.		Ethyl Alcohol
Product Type 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.		Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.		Sc Johnson Professional Usa, Inc.
Labeler Code11084
FDA Application Number 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.		part333E
Marketing Category 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.		OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		05-15-2012
Listing Expiration Date 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.		12-31-2023
Exclude Flag 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". 		N
NDC Code Structure

What are the uses for Appeal Alcohol Foaming Hand Sanitizer?


Product Packages

NDC Code 11084-702-27

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

Product Details

What are Appeal Alcohol Foaming Hand Sanitizer Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Appeal Alcohol Foaming Hand Sanitizer Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

Appeal Alcohol Foaming Hand Sanitizer 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.

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Appeal Alcohol Foaming Hand Sanitizer Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Otc - Active Ingredient



Active ingredient

Ethyl Alcohol 70% ww


Otc - Purpose



Purpose

Antibacterial


Indications & Usage



Uses

For hand sanitizing to reduce bacteria on the skin


Warnings



Warnings

For external use only

Flammable: Keep away from fire or flame.


Otc - When Using



When using this product avoid contact with eyes.  In case of eye contact, flush with water.


Otc - Keep Out Of Reach Of Children



Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.


Dosage & Administration



Directions

Apply one shot of foaming sanitizer to dry hands

Rub into skin

No rinsing required


Inactive Ingredient



Inactive ingredients

Water, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chlroide


Package Label.Principal Display Panel



APP17102

102668

appeal Alcohol Foaming Hand Sanitizer

Certified EcoLogo

Certified Instant Hand Antiseptic CCD-170

1 Liter

33.8 Fluid Ounces

Made in Canada by Deb

deb foam technolody

Distributed exclusively by:

Interline Brands

Jacksonville, FL  32207

www.AppealProducts.com

Rev. 05-12

01830


* Please review the disclaimer below.