NDC 76370-0011 Cleanse Wise Antibacterial Hand Wipes

Benzalkonium Chloride

NDC Product Code 76370-0011

NDC 76370-0011-0

Package Description: 35 APPLICATOR in 1 CANISTER > 4 mL in 1 APPLICATOR

NDC Product Information

Cleanse Wise Antibacterial Hand Wipes with NDC 76370-0011 is a a human over the counter drug product labeled by Terraboost Media Llc. The generic name of Cleanse Wise Antibacterial Hand Wipes is benzalkonium chloride. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Terraboost Media Llc

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.

Cleanse Wise 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.


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)
  • C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)

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: Terraboost Media Llc
Labeler Code: 76370
FDA Application Number: part333E 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: 05-12-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Cleanse Wise Antibacterial Hand Wipes Product Label Images

Cleanse Wise 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


Drug Facts

Terraboost Media, LLC

3109 Grand Avenue #300
Miami, FL 33133A product of Terraboost®877-837-7210www.tazzabrands.comMADE IN USA WITH GLOBAL MATERIALS

Otc - Active Ingredient

Active ingredientBenzalkonium chloride 0.13%

Otc - Purpose


Indications & Usage

  • Usesto decrease bacteria on the skinrecommended for repeated use


WarningsFor external use only

Otc - When Using

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Dosage & Administration

  • Directionsrub wipe thoroughly over all surfaces of both handsallow to dry without wipingsupervise children under 6 years oldnot recommended for infantsdispose of wipe in trash; do not flush

Inactive Ingredient

Inactive ingredientsWater, Fragrance, C12-15 Alcohols, Chloroxylenol, Aloe Barbadensis Leaf Juice

* Please review the disclaimer below.