NDC 72728-002 Sterile Alcohol Prep Pads

Sterile Alcohol Prep Pads

NDC Product Code 72728-002

NDC Code: 72728-002

Proprietary Name: Sterile Alcohol Prep Pads 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.

Non-Proprietary Name: Sterile Alcohol Prep Pads 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.


Code Structure
  • 72728 - A2z Products, Llc
    • 72728-002 - Sterile Alcohol Prep Pads

NDC 72728-002-00

Package Description: 1 SWAB in 1 PACKET

NDC 72728-002-01

Package Description: 100 SWAB in 1 BOX

NDC 72728-002-02

Package Description: 1 SWAB in 1 BOX

NDC 72728-002-03

Package Description: 300 SWAB in 1 BOX

NDC 72728-002-04

Package Description: 400 SWAB in 1 BOX

NDC 72728-002-05

Package Description: 500 SWAB in 1 BOX

NDC Product Information

Sterile Alcohol Prep Pads with NDC 72728-002 is a a human over the counter drug product labeled by A2z Products, Llc. The generic name of Sterile Alcohol Prep Pads is sterile alcohol prep pads. The product's dosage form is swab and is administered via topical form.

Labeler Name: A2z Products, Llc

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab 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.


Sterile Alcohol Prep Pads 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.

  • ISOPROPYL ALCOHOL .7 mL/1
  • ISOPROPYL ALCOHOL .7 mL/1
  • ISOPROPYL ALCOHOL .7 mL/1
  • ISOPROPYL ALCOHOL .7 mL/1
  • ISOPROPYL ALCOHOL .7 mL/1
  • ISOPROPYL ALCOHOL .7 mL/1

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.
  • 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.
  • 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: A2z Products, Llc
Labeler Code: 72728
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: 02-15-2019 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: 12-31-2020 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.

Sterile Alcohol Prep Pads Product Label Images

Sterile Alcohol Prep Pads 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

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic, Sterile Solution

Uses

Antiseptic cleanserKills harmful bacteria and germsFirst aid to help prevent infection

Warnings

For External Use OnlyAvoid contact with the eyesIf contact occurs, flush eyes with water

Do Not Use

With electrocautery prodeduresIn the eyes

Stop Use And Ask A Doctor If

Irritation and redness developsIf condition persists for more than 72 hours, consult a physician

Discontinue Use And Consult A Healthcare Practitioner If

Irritation develops

Keep Out Of Reach Of Children

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

Directions

Use as part of your daily cleansing routineMay be covered with a sterile bandage

Other Information

Store at room temperature 15°-30°C (59°-86°F)Avoid excessive heat

Inactive Ingredients

Water

* Please review the disclaimer below.

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