NDC 73118-001 Povidone-iodine Prep Pad

Povidone-iodine

NDC Product Code 73118-001

NDC Code: 73118-001

Proprietary Name: Povidone-iodine Prep Pad 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: Povidone-iodine 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.

NDC Code Structure

  • 73118 - Nantong Furuida Packaging Products Co., Ltd.
    • 73118-001 - Povidone-iodine Prep Pad

NDC 73118-001-01

Package Description: 200 PACKAGE in 1 BOX > 1 SWAB in 1 PACKAGE

NDC Product Information

Povidone-iodine Prep Pad with NDC 73118-001 is a a human over the counter drug product labeled by Nantong Furuida Packaging Products Co., Ltd.. The generic name of Povidone-iodine Prep Pad is povidone-iodine. The product's dosage form is swab and is administered via percutaneous form.

Labeler Name: Nantong Furuida Packaging Products Co., Ltd.

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.

Povidone-iodine Prep Pad 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.

  • POVIDONE-IODINE 10 mg/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.

  • Percutaneous - Administration through the skin.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nantong Furuida Packaging Products Co., Ltd.
Labeler Code: 73118
FDA Application Number: part333C 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 05-27-2019 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.

Povidone-iodine Prep Pad Product Label Images

Povidone-iodine Prep Pad 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

POVIDONE-IODINE 10% W/v (equivalent to iodine 1%)

Purpose

Antiseptic

Warnings

For External use only.











Discontinue use if irritation and redness develop

Keep Out Of Reach Of Children

Keep out of reach of children

Directions

Apple locally as needed.

Other Information

Store at room temperature:59o-86oF(15--30℃)

Use

Antiseptic for preparation of the skin

Inactive Ingredients

Purified Water

* Please review the disclaimer below.

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