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  4. NDC Product Code: 52486-001 Para-aid Povidone-iodine Prep Pads

NDC 52486-001 Para-aid Povidone-iodine Prep Pads

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52486-001?
  5. Para-aid Povidone-iodine Prep Pads Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52486-001
Proprietary Name:
Para-aid Povidone-iodine Prep Pads
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mcure Health Solutions Inc.
Labeler Code:
52486
Product Label ID:
2ad05cb6-8663-3474-e054-00144ff88e88
Start Marketing Date: [9]
02-02-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Code Structure Chart

Product Details

What is NDC 52486-001?

The NDC code 52486-001 is assigned by the FDA to the product Para-aid Povidone-iodine Prep Pads which is product labeled by Mcure Health Solutions Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52486-001-01 10 ml in 1 packet . 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 Para-aid Povidone-iodine Prep Pads?

Wipe surgery site vigorously and discard.

Which are Para-aid Povidone-iodine Prep Pads UNII Codes?

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

Which are Para-aid Povidone-iodine Prep Pads 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:

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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".