NDC 77720-018 Hand Sanitizer

Ethyl Alcohol

NDC Product Code 77720-018

NDC 77720-018-01

Package Description: 30 BOTTLE in 1 CARTON > 237 mL in 1 BOTTLE

NDC Product Information

Hand Sanitizer with NDC 77720-018 is a a human over the counter drug product labeled by Skaffles Group Limited Liability Company. The generic name of Hand Sanitizer is ethyl alcohol. The product's dosage form is spray and is administered via topical form.

Labeler Name: Skaffles Group Limited Liability Company

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Hand Sanitizer 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 71 mL/100mL

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: Skaffles Group Limited Liability Company
Labeler Code: 77720
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: 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.

Hand Sanitizer Product Label Images

Hand Sanitizer 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 71%




Hand sanitizing to help reduce bacteria on the skin. Recommended for repeated use.


For external use only./ Para uso externo uinicamente.

Do not use / No utilice o lf you are allergic to any of the ingredients. o In the eyes;if contact occurs, rinse thoroughly with water.i Si es alergico a alguno de losingredientes.· Si entra en contacto con los ojos,enjuague por completo con agua.Discontinue use ifiritation and redness develop. lf condition persists for morethan 72 hours consult a doctor./Suspenda el uso si se presenta irritacion yenrojecimiento.Consulte a un medico si la condicion persiste por mas de 72 horas.Keep out of reach of children. If swallowed, get medical help or contact aPoison Control Center right away./ Mantengase fuera del alcance de los niios.Sise ingiere, obtenga atencion medica o pongase en contacto de inmediato conun Centro de control de envenenamientos.

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.


Adtults and children 2 yrs and over, apply to hands and allow skin to dry without wiping. Children under 2, ask doctor before use.

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Propylene Glycol, TocopheryI Acetate (Vitamin E), Triethanolamine, Water(Aqua).

* Please review the disclaimer below.