NDC 50663-003 Hand Sanitizer-gel

Dial Professional Gel Hand Sanitizer

NDC Product Code 50663-003

NDC 50663-003-01

Package Description: 118 mL in 1 BOTTLE

NDC 50663-003-02

Package Description: 221 mL in 1 BOTTLE, PUMP

NDC 50663-003-03

Package Description: 443 mL in 1 BOTTLE, PUMP

NDC 50663-003-04

Package Description: 473 mL in 1 CELLO PACK

NDC 50663-003-05

Package Description: 800 mL in 1 CELLO PACK

NDC Product Information

Hand Sanitizer-gel with NDC 50663-003 is a a human over the counter drug product labeled by Zotos International Inc. The generic name of Hand Sanitizer-gel is dial professional gel hand sanitizer. The product's dosage form is gel and is administered via topical form.

Labeler Name: Zotos International Inc

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Hand Sanitizer-gel 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.

  • ALCOHOL 60.146532 mL/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)
  • WATER (UNII: 059QF0KO0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • TERT-BUTYL ALCOHOL (UNII: MD83SFE959)

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.
  • 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: Zotos International Inc
Labeler Code: 50663
FDA Application Number: part356 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: 05-01-2020 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: 12-31-2021 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.

Hand Sanitizer-gel Product Label Images

Hand Sanitizer-gel 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(S)

Ethyl Alcohol 62% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from fire or flame

Otc - When Using

When using this product keep avoid contact with face, eyes, and broken skin. if eye contact occurs, flush thoroughly with water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

Directions

Wet hands thoroughly with product and rub into skin until dry.Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredients

Aqua (Water, Eau)• Propylene Glycol• Glycerin• Carbomer • Aminomethyl Propane! • lsopropyl Myrlstate • T-Butyl Alcohol

Questions

? 1-877-777-3277

®,TM,©2018 Distributed by

Henkel Corporation,

Rocky Hill, CT 06067

www.dialprofessional.com

* Please review the disclaimer below.