NDC 72005-015 Toys Story Cotton Candy Scented Hand Sanitizer 01

Benzalkonium Chloride

NDC Product Code 72005-015

NDC Code: 72005-015

Proprietary Name: Toys Story Cotton Candy Scented Hand Sanitizer 01 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

  • 72005 - Townley Inc.
    • 72005-015 - Toys Story Cotton Candy Scented Hand Sanitizer

NDC 72005-015-01

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Toys Story Cotton Candy Scented Hand Sanitizer 01 with NDC 72005-015 is a a human over the counter drug product labeled by Townley Inc.. The generic name of Toys Story Cotton Candy Scented Hand Sanitizer 01 is benzalkonium chloride. The product's dosage form is gel and is administered via topical form.

Labeler Name: Townley 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.

Toys Story Cotton Candy Scented Hand Sanitizer 01 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.

  • COCETH-7 (UNII: 58Y261JLH5)
  • PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
  • WATER O-18 (UNII: 7QV8F8BYNJ)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOMER 934 (UNII: Z135WT9208)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • MYRISTICA FRAGRANS FRUIT (UNII: GOO22BTU71)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • COCETH-7 (UNII: 58Y261JLH5)
  • PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
  • CARBOMER 934 (UNII: Z135WT9208)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • WATER O-18 (UNII: 7QV8F8BYNJ)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • MYRISTICA FRAGRANS FRUIT (UNII: GOO22BTU71)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
  • COCETH-7 (UNII: 58Y261JLH5)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • MYRISTICA FRAGRANS FRUIT (UNII: GOO22BTU71)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • WATER O-18 (UNII: 7QV8F8BYNJ)
  • CARBOMER 934 (UNII: Z135WT9208)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)

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: Townley Inc.
Labeler Code: 72005
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: 06-06-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 06-06-2022 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Toys Story Cotton Candy Scented Hand Sanitizer 01 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 Purpose

Benzalkonium chloride 0.1% Antibacterial

Use

To decrease bacteria on the skin that could cause disease.

Warnings

For external use only-handskeep out of eyes- avoid contact with broken skinStop use and ask a dosctor if irritation or radness developsDo not inhale or ingest. If swallowed, get medical help or contact a poison control right away.

Direction

Rub a dime sized drop into hands.

Otc - Keep Out Of Reach Of Children

For children under 6 use under adult supervision

Inactive Ingredients

INACTIVE INGREDIENTS: WATER, GLYCERIN, COCETH-7, PPG-1-PEG-9 LAURYL GLYCOL ETHER, CARBOMER, SODIUM HYDROXIDE, PEG-40 HYDROGENATED CASTOR OIL, FRAGRANCE (PARFUM).




MAY CONTAIN: RED 40, RED 33, BLUE 1, YELLOW 5.

Questions?

1-212-779-0544 weekdays

* Please review the disclaimer below.