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  4. NDC Product Code: 42339-002 Povidone-iodine Pad

NDC 42339-002 Povidone-iodine Pad

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42339-002?
  4. Povidone-iodine Pad Uses
  5. Active Ingredients UNII Codes
  6. 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:
42339-002
Proprietary Name:
Povidone-iodine Pad
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shandong Haiyan Medical Manufacture Co., Ltd.
Labeler Code:
42339
Product Label ID:
a1c21c1a-d316-4294-ba74-8d82c9092ee3
Start Marketing Date: [9]
02-18-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 42339-002-01

Package Description: 10 BOX in 1 CONTAINER / 100 POUCH in 1 BOX / .6 g in 1 POUCH

NDC Code 42339-002-02

Package Description: 100 BOX in 1 CONTAINER / 100 POUCH in 1 BOX / .6 g in 1 POUCH

Product Details

What is NDC 42339-002?

The NDC code 42339-002 is assigned by the FDA to the product Povidone-iodine Pad which is product labeled by Shandong Haiyan Medical Manufacture Co., Ltd.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 42339-002-01 10 box in 1 container / 100 pouch in 1 box / .6 g in 1 pouch, 42339-002-02 100 box in 1 container / 100 pouch in 1 box / .6 g 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 Pad?

Apply locally as needed.Other InformationStore at room temperature: 59°- 86°F(15 - 30℃)

Which are Povidone-iodine Pad UNII Codes?

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

Which are Povidone-iodine Pad 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".