NDC 80614-005 V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol
Alcohol Gel Topical

Product Information

What is NDC 80614-005?

The NDC code 80614-005 is assigned by the FDA to the product V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol which is a human over the counter drug product labeled by Scalpi Cosmetica S.a. The generic name of V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol is alcohol. The product's dosage form is gel and is administered via topical form. The product is distributed in 2 packages with assigned NDC codes 80614-005-01 150 pouch in 1 box / 1.5 ml in 1 pouch, 80614-005-02 250 pouch in 1 box / 1.5 ml in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code80614-005
Proprietary Name 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.		V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol
Non-Proprietary Name 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.		Alcohol
Product Type 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.		Human Otc Drug
Dosage FormGel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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.		Scalpi Cosmetica S.a
Labeler Code80614
FDA Application Number 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.		part333E
Marketing Category 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.		OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		09-01-2020
Listing Expiration Date 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.		12-31-2023
Exclude Flag 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". 		N
NDC Code Structure

What are the uses for V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol?


Product Packages

NDC Code 80614-005-01

Package Description: 150 POUCH in 1 BOX / 1.5 mL in 1 POUCH

NDC Code 80614-005-02

Package Description: 250 POUCH in 1 BOX / 1.5 mL in 1 POUCH

Product Details

What are V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol Inactive Ingredients UNII Codes

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.

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V-shapes Antiseptic Hand Sanitizer Ethyl Alcohol Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Drug Facts




Active Ingredient



Ethyl alcohol 70%


Purpose



Antiseptic


Uses



  • For hand washing to decrease bacteria on the skin 
  • recommended for repeated use

Warnings



For external use only

Flammable, keep away from fire or flame.


Do Not Use



in the eyes


Stop Use And Ask A Doctor If



  • irritation and redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children.



If swallowed, get medical help or contact a Poison Control Center right away.


Directions



Wet hands thoroughly with product and allow to dry without wiping


Inactive Ingredients



Acrylates/C10-C30 Alkyl Acrylate Crosspolymer, Triethanolamine, Water


Questions Or Comments?



1-800-783-1224


Package Labeling:150Sachets



Bottle - Bottle

Bottle - Bottle


Package Labeling:250Sachets



Box3 - Box3

Box3 - Box3


* Please review the disclaimer below.