NDC 59050-250 Povidone-iodine Gel Swabstick Non-sterile

Povidone Iodine

NDC Product Information

Povidone-iodine Gel Swabstick Non-sterile with NDC 59050-250 is a a human over the counter drug product labeled by Changzhou Maokang Medical Products Co. Ltd. The generic name of Povidone-iodine Gel Swabstick Non-sterile is povidone iodine. The product's dosage form is gel and is administered via topical form.

Labeler Name: Changzhou Maokang Medical Products Co. Ltd

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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 Gel Swabstick Non-sterile 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/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.

  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • WATER (UNII: 059QF0KO0R)
  • NONOXYNOL-10 (UNII: K7O76887AP)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) (UNII: X70SE62ZAR)
  • POTASSIUM IODIDE (UNII: 1C4QK22F9J)
  • 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: Changzhou Maokang Medical Products Co. Ltd
Labeler Code: 59050
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: 11-05-2019 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 Gel Swabstick Non-sterile Product Label Images

Povidone-iodine Gel Swabstick Non-sterile 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 USP 10%

Purpose

Antiseptic

Use

Antiseptic skin preparation

Do Not Use

  • If allergic to Iodinein the eyes

Stop Use And Ask A Doctor If

  • Rednes, irritation, swelling or pain persists or increasesinfection occurs

Keep Out Of Reach Of Children

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.Avoid pooling beneath the patient

Ask A Doctor Before Use If Injuries Are

  • Deep puncture woundsserious burns

Directions

Apply product to skin as needed

Other Information

  • 1% titratablefor hospital or professional use only

Inactive Ingredients

Citric Acid, Alkyl Glucoside, Hydroxyethyl Cellulose, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water

* Please review the disclaimer below.