NDC 79589-001 Sanitizing Wipes

Alcohol

NDC Product Code 79589-001

NDC 79589-001-01

Package Description: 50 PATCH in 1 PACKAGE > 5 g in 1 PATCH

NDC Product Information

Sanitizing Wipes with NDC 79589-001 is a a human over the counter drug product labeled by Arch Point Group Llc. The generic name of Sanitizing Wipes is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Arch Point Group 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.

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 .75 mL/g

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)
  • GLYCERIN (UNII: PDC6A3C0OX)

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: Arch Point Group Llc
Labeler Code: 79589
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: 07-09-2020 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.

Sanitizing Wipes Product Label Images

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

Otc - Active Ingredient

Alcohol 75%. Purpose: Antiseptic

Otc - Purpose

Antiseptic

Use(S)

Single Use Wipes for Hands

Warning

  • For external use only; hands, general cleansing.Does not replace wipes used for medical procedures.Flammable; Keep away from fire or flameDo not ingest

When Using This Product

  • Keep our of eyes. In case of contact with eyes, flush thoroughly with water.Avoid contact with broken skin.

Do Not Use

On open skin wounds

Stop Use And Ask A Doctor If

  • Irritation and redness developcondition persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep our of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

Close properly after dispensing to maintain purity, as alcohol by nature evaporates quickly.

Dispose of properly, DO NOT FLUSH

Other Information

  • Keep out of light; store at room temperature 59F-86F. Close properly after dispensing to maintain purity, as alcohol by nature evaporates quickly.Dispose of properly, DO NOT FLUSH.

Inactive Ingredients

Water, Glycerol

* Please review the disclaimer below.