NDC 42129-106 You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented

Alcohol Wipes

NDC Product Code 42129-106

NDC CODE: 42129-106

Proprietary Name: You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented 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: Alcohol Wipes 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

  • 42129 - Fustin(xiamen) Commodity Co., Ltd
    • 42129-106 - You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented

NDC 42129-106-01

Package Description: 50 CLOTH in 1 BAG

NDC Product Information

You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented with NDC 42129-106 is a a human over the counter drug product labeled by Fustin(xiamen) Commodity Co., Ltd. The generic name of You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented is alcohol wipes. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Fustin(xiamen) Commodity 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.

You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented 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 75 1/1001

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • TOCOPHEROL (UNII: R0ZB2556P8)

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: Fustin(xiamen) Commodity Co., Ltd
Labeler Code: 42129
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: 10-19-2020 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.

You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented Product Label Images

You Are A Magical Unicorn Antibacterial Hand Sanitizer Wipes Cotton Candy Scented 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

Ethyl Alcohol 75%

Purpose

Antiseptic

Warnings

For external use only. Flammable. Keep away from fire or flame. When using this product Avoid contact with eyes; in case of contact, flush eyes with water.Stop use and ask a doctor if irritation and redness develop and persists.

Indications & Usage

Decrease bacteria on hands

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 htoroughly with product and allow to dry.

Inactive Ingredients

Water, Glycerin, Fragrance (Parfum), Benzalkonium Chloride, Tocopherol, Aloe Barbadensis Leaf Extract.

* Please review the disclaimer below.