NDC 74707-500 Alchohol Wipes

Alcohol Wipes

NDC Product Code 74707-500

NDC 74707-500-10

Package Description: 1 g in 1 BAG

NDC Product Information

Alchohol Wipes with NDC 74707-500 is a a human over the counter drug product labeled by Virus Protection Systems Llc. The generic name of Alchohol Wipes is alcohol wipes. The product's dosage form is cloth and is administered via extracorporeal; topical form.

Labeler Name: Virus Protection Systems 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.

Alchohol 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 g/100g

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 O-15 (UNII: 63M8RYN44N)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Extracorporeal - Administration outside of the body.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Extracorporeal - Administration outside of the body.
  • 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: Virus Protection Systems Llc
Labeler Code: 74707
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: 09-01-2020 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.

Alchohol Wipes Product Label Images

Alchohol 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

Acohol 75% By Volume

Alcohol 75% by volume........Antispetic

Warnings Section

Flammable keep away from flame and fireFor external use onlyWhen using this product do not get in the eyes, if contact occurs rinse throughly with waterDicontinue use if irritaton and redeness devvelop.If conditions persist for more than 72 hours consult a doctorkeep this out of reach of childrenif swallowed, get medical help or contact a poison control center right away

Uses Section

Hand Sanitizer Wipe to decrease bacteria on the skinDries in Seconds

Directions

Apply to handAllow to dry without wiping

Inactive Ingredient

Aloe Barbadensis Leaf JuiceGlycerinPropyleneGlycolTocopherylWater

Dosage & Administration

Apply to handsAplly tyo dry without wiping

Indications & Usage

Hand Sanitizer wipe to decrease bacteria on the skinDries in seconds

Otc - Keep Out Of Reach Of Children

Keep this out of reach of children

* Please review the disclaimer below.