NDC 80744-001 Sanko Sanitizing Wipes


NDC Product Code 80744-001

NDC 80744-001-01

Package Description: 100 APPLICATOR in 1 POUCH > 4.2 mL in 1 APPLICATOR

NDC Product Information

Sanko Sanitizing Wipes with NDC 80744-001 is a a human over the counter drug product labeled by Harper + Scott Llc. The generic name of Sanko Sanitizing Wipes is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Harper + Scott 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.

Sanko Sanitizing 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.

  • ALCOHOL 70 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.
  • 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: Harper + Scott Llc
Labeler Code: 80744
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: 10-02-2020 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.

Sanko Sanitizing Wipes Product Label Images

Sanko Sanitizing 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

Made in China.Distributed by Harper and Scott, LLC915 Broadway New York, NY 10010www.shopsanko.comKills most germs without water. Personal safety for every person.
100 Soft Wipes: 7.87" x 5.90" (20 cm x 15 cm)
This product is made of spunlaced non-woven fabric and should not be flushed down the toilet into any sewer system.

Otc - Active Ingredient

Active IngredientAlcohol 70% v/v

Otc - Purpose


Indications & Usage

Use For sanitizing to decrease bacteria on the skin. For use when soap and water are not available.


WarningsFor external use only.Flammable, keep away from fire or flame.

Otc - When Using

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Otc - Stop Use

Discontinue use if irritation and redness develops. If condition persists for more than 72 hours consult a doctor.

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. 1-800-222-1222

Dosage & Administration

  • DirectionsOpen packet, remove and unfold pre-moistened tissue.Wipe hands and allow to dry without wiping.Discard properly after single use.Do not flush down toilet.

Storage And Handling

  • Other InformationStore at room temperature. Keep out of direct sunlight.

Inactive Ingredient

Inactive IngredientsWater, Glycerol.

* Please review the disclaimer below.