NDC 76370-0004 Tazza


NDC Product Code 76370-0004

NDC 76370-0004-0

Package Description: 40 CLOTH in 1 POUCH

NDC 76370-0004-1

Package Description: 250 CLOTH in 1 CANISTER

NDC 76370-0004-2

Package Description: 1500 CLOTH in 1 BAG

NDC 76370-0004-3

Package Description: 1200 CLOTH in 1 BAG

NDC 76370-0004-4

Package Description: 240 CLOTH in 1 CANISTER

NDC 76370-0004-5

Package Description: 160 CLOTH in 1 POUCH

NDC 76370-0004-6

Package Description: 80 CLOTH in 1 POUCH

NDC 76370-0004-7

Package Description: 20 CLOTH in 1 POUCH

NDC 76370-0004-8

Package Description: 50 CLOTH in 1 POUCH

NDC 76370-0004-9

Package Description: 100 CLOTH in 1 POUCH

NDC Product Information

Tazza with NDC 76370-0004 is a a human over the counter drug product labeled by Terraboost Media Llc. The generic name of Tazza is ethanol. The product's dosage form is cloth and is administered via topical form.

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.

Tazza 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)

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: 08-02-2016 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 - 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.

Tazza 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

Manufactured for Terraboost Media, LLC3109 Grand Avenue #300Miami, FL 33133A Product of Terraboost®877-837-7210 • www.tazzabrands.com

Otc - Active Ingredient

Active ingredient
Ethanol 70%

Otc - Purpose


Indications & Usage

  • Usesfor hand sanitizing to decrease bacteria on the skinrecommended for repeated use


WarningsFor external use onlyFlammable. Keep away from fire or flame.

Otc - When Using

When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develop

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.

Dosage & Administration

  • Directionstake wipe and rub thoroughly over all surfaces of both handsrub hands together briskly to drydispose of wipe

Inactive Ingredient

Inactive ingredientsPurified Water, Vegetable Glycerin, Lavendula Angustifolia (Lavender) Essential Oil, Organic Aloe Barbadensis Leaf Extract, Organic Matricaria Recutita (Chamomile) Flower Extract

* Please review the disclaimer below.