NDC 77465-003 Disney Frozen Ii Antibacterial Hand Wipes

Benzalkonium Chloride

NDC Product Code 77465-003

NDC CODE: 77465-003

Proprietary Name: Disney Frozen Ii Antibacterial Hand Wipes 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

  • 77465 - Zhejiang Youquan Care Products Technology Co., Ltd.
    • 77465-003 - Disney Frozen Ii Antibacterial Hand Wipes

NDC 77465-003-01

Package Description: 20 NOT APPLICABLE in 1 POUCH > 63 g in 1 NOT APPLICABLE

NDC Product Information

Disney Frozen Ii Antibacterial Hand Wipes with NDC 77465-003 is a a human over the counter drug product labeled by Zhejiang Youquan Care Products Technology Co., Ltd.. The generic name of Disney Frozen Ii Antibacterial Hand Wipes is benzalkonium chloride. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Zhejiang Youquan Care Products Technology 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.

Disney Frozen Ii Antibacterial Hand Wipes 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 .13 g/100g

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.

  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • WATER (UNII: 059QF0KO0R)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)

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: Zhejiang Youquan Care Products Technology Co., Ltd.
Labeler Code: 77465
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: 01-25-2021 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 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.

Disney Frozen Ii Antibacterial Hand Wipes Product Label Images

Disney Frozen Ii Antibacterial Hand Wipes 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%.

Purpose

Antibacterial

Use

Decreases bacteria on skin

Warning

For external use only

Do not use if you are allergic to any ingredients When using this product do not get into your eyes. lf contact occurs, rinse thoroughly with water.

Use of this product by children should be supervised by an adult.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep this out of reach of children.f swallowed, get medical help

or contact a Poison Control Center immediately.

Directions

Adults and children 2 years and over

·Apply to hands

·Allow to dry without wiping

children under 2 years

ask a doctor before use

Inactive Ingredients

Water, Phenoxyethanol, Propylene Glycol, Glycerin, Ethylhexylglycerin, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate.

* Please review the disclaimer below.