NDC 50730-8201 Povidone Iodine Plus

NDC Product Code 50730-8201

NDC CODE: 50730-8201

Proprietary Name: Povidone Iodine Plus 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.

NDC Code Structure

  • 50730 - H And P Industries, Inc. Dba Triad Group

NDC 50730-8201-8

Package Description: 1 g in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Povidone Iodine Plus with NDC 50730-8201 is a product labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 312563.

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
  • POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Labeler Information

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

Labeler Name: H And P Industries, Inc. Dba Triad Group
Labeler Code: 50730
Start Marketing Date: 05-01-2001 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Povidone Iodine Plus Product Label Images

Povidone Iodine Plus 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% (equivalent to 1% titratable iodine)

Purpose

Antiseptic

Use

First Aid Antiseptic to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do Not Use

  • In the eyes or over large areas of the bodylonger than 1 week unless directed by a doctor

Stop Use And Ask A Doctor

  • If condition persists or gets worsein case of deep puncture wounds, animal bites or serious burns

Keep Out Of Reach Of Children

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

Directions

Clean the affected area. Apply a small amount of this product to the area 1-3 times daily. May be covered with a sterile bandage.

Other Information

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

Inactive Ingredients

Glycerin, PEG-300, PEG-1450, propylene glycol

Package Information

  • TRIADCat. No. 11-OP01NDC 50730-8201-8POVIDONE IODINEOINTMENT10% Povidone Iodine, USP(equivalent to 1% titratable iodine)First Aid AntisepticFor Hospital and Professional Use OnlyTriad Group, Inc.300 West North Shore DriveHartland, WI 53029www.triad-group.netNet Wt. 1 gram

* Please review the disclaimer below.