NDC 77731-001 Brookstone Antibacterial Hand Wipes Fresh Scent

Benzalkonium Chloride

NDC Product Code 77731-001

NDC 77731-001-01

Package Description: 1 SOLUTION in 1 BAG

NDC 77731-001-02

Package Description: 20 SOLUTION in 1 BAG

NDC 77731-001-03

Package Description: 50 SOLUTION in 1 BAG

NDC 77731-001-04

Package Description: 100 SOLUTION in 1 BAG

NDC Product Information

Brookstone Antibacterial Hand Wipes Fresh Scent with NDC 77731-001 is a a human over the counter drug product labeled by Argento Sc By Sicura Inc.. The generic name of Brookstone Antibacterial Hand Wipes Fresh Scent is benzalkonium chloride. The product's dosage form is solution and is administered via topical form.

Labeler Name: Argento Sc By Sicura Inc.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

Brookstone Antibacterial Hand Wipes Fresh Scent 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 .008 g/1

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
  • GLYCERIN (UNII: PDC6A3C0OX)

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: Argento Sc By Sicura Inc.
Labeler Code: 77731
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: 05-26-2020 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.

Brookstone Antibacterial Hand Wipes Fresh Scent Product Label Images

Brookstone Antibacterial Hand Wipes Fresh Scent 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)

Benzalkonium Chloride 0.2%

Otc - Purpose

Purpose: Disinfectant

Use

Decrease bacteria on skin that could cause diseaseRecommended for repeated use

Warnings

For external use only. Flammable, keep way from flame or fire

When Using This Product

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with waterDo not ingest or inhaleAvoid contact with broken skin

Stop Use And Ask A Doctor

If irrigation and redness develop and condition persists for more than 72 hours

Keep Out Of Reach Of Children

If swallowed,get medical help or contact a Poison Control Center immediately

Directions

  • Wipe product on hands thoroughly and allow to dry, do not wipe offFor children under 6, use under adult supervisionNot recommended for use with infants

Other Information

Do not store above 105F (40.6C)May discolor some fabricsHarmful to plastics and wood finishes

Inactive Ingredients

Purified water, Phenoxyethanol, Ethylhexylglycerin, Didecyldimonium Chloride, PropyleneGlycol, Glycerin, Fragrance

* Please review the disclaimer below.