NDC 79248-031 Tarocco Hand Sanitizer Sicilian Blood Oranges


NDC Product Code 79248-031

NDC 79248-031-04

Package Description: 120 mL in 1 BOTTLE

NDC Product Information

Tarocco Hand Sanitizer Sicilian Blood Oranges with NDC 79248-031 is a a human over the counter drug product labeled by Cali Cosmetics, Inc.. The generic name of Tarocco Hand Sanitizer Sicilian Blood Oranges is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Cali Cosmetics, 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.

Tarocco Hand Sanitizer Sicilian Blood Oranges 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.

  • ALCOHOL .72 mL/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)

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: Cali Cosmetics, Inc.
Labeler Code: 79248
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: 12-30-2020 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.

Tarocco Hand Sanitizer Sicilian Blood Oranges Product Label Images

Tarocco Hand Sanitizer Sicilian Blood Oranges 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

Ethyl Alcohol 72% (v/v)




  • To help reduce bacteria on the skin.


  • For external use only.Flammable.Keep away from fire or flame.

When Using This Product

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop Using And Ask A Doctor If

  • Irritation or redness develops and lasts.

Keep Out Of Reach Of Children

  • In case of accidental ingestion, get medical help or contact a poison control center immediately.


  • Spray onto the palms of your hands and rub together until spray is absorbed.

Other Information

  • Store below 110°F (43°C).

Inactive Ingredients

Aqua (Water), Glycerin, Hydrolyzed Jojoba Esters, Parfum(Fragrance), Aloe Barbadensis Leaf Juice, Olea Europaea (Olive) Fruit Oil Citrus Aurantium Dulcis (Orange) Fruit Extract

* Please review the disclaimer below.