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  4. NDC Product Code: 63517-132 Povidone Iodine Prep

NDC 63517-132 Povidone Iodine Prep

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63517-132?
  4. Povidone Iodine Prep Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63517-132
Proprietary Name:
Povidone Iodine Prep
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
63517
Product Label ID:
4c47327a-3d31-4cf3-ae81-6a20976197fb
Start Marketing Date: [9]
08-26-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 63517-132?

The NDC code 63517-132 is assigned by the FDA to the product Povidone Iodine Prep which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63517-132-01 500 pouch in 1 case / 22.2 ml in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Povidone Iodine Prep?

Clean the affected area.For preparation of skin prior to surgeryApply product to the operative site prior to surgeryFor first aid antisepticApply a small amount of this product on the area 1-3 times daily.May be covered with a sterile bandage.If bandaged, let dry first.

Which are Povidone Iodine Prep UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Povidone Iodine Prep Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Povidone Iodine Prep?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".