NDC 73741-104 Kiss My Face Hand Sanitizer Fragrance Free

Benzalkonium Chloride

NDC Product Code 73741-104

NDC CODE: 73741-104

Proprietary Name: Kiss My Face Hand Sanitizer Fragrance Free 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

  • 73741 - Cemi International, Inc
    • 73741-104 - Kiss My Face Hand Sanitizer Fragrance Free

NDC 73741-104-02

Package Description: 502 mL in 1 BOTTLE, PUMP

NDC Product Information

Kiss My Face Hand Sanitizer Fragrance Free with NDC 73741-104 is a a human over the counter drug product labeled by Cemi International, Inc. The generic name of Kiss My Face Hand Sanitizer Fragrance Free is benzalkonium chloride. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Cemi International, Inc

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Kiss My Face Hand Sanitizer Fragrance Free 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 1.3 mg/mL

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)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • LAURETH-7 (UNII: Z95S6G8201)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

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: Cemi International, Inc
Labeler Code: 73741
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: 07-16-2020 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.

Kiss My Face Hand Sanitizer Fragrance Free Product Label Images

Kiss My Face Hand Sanitizer Fragrance Free 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

Antimicrobial

Indications & Usage

Uses: • For antiseptic cleansing to decrease bacteria on the skin. Reccomended for repeated use.

Warnings

Warnings:For external use only.When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.Ask a doctor: Stop useand consult a doctor if irritation or redness develops. If condition persists for more than 72 hours, discontinue use.Do not use on children less than 2 months of age or on open skin wounds.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

Directions: Apply a small amount of gel into palm of hand. Rub thoroughly over all surfaces of both hands for 15 seconds.

Storage And Handling

Other information Store tightly closed, in a cool dry place.

Inactive Ingredient

Inactive ingredients Water, ​​Aloe barbadensis Leaf Extract, Sodium Hyaluronate, Cocos nucifera (Coconut) Oil, Glycerin, Polyacrylamide, Tocopheryl Acetate, Propylene Glycol, Polyquaternium-7, Polysorbate 20, C13-14 Isoparaffin, Laureth-7, Phenoxyethanol, Aminomethyl Propanol

* Please review the disclaimer below.