NDC 34645-4001 Povidone-iodine

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
34645-4001
Proprietary Name:
Povidone-iodine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangsu Province Jianerkang Medical Dressing Co. ,ltd.
Labeler Code:
34645
Start Marketing Date: [9]
01-01-2008
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 34645-4001-4

Package Description: 5.5 mL in 1 POUCH

Product Details

What is NDC 34645-4001?

The NDC code 34645-4001 is assigned by the FDA to the product Povidone-iodine which is product labeled by Jiangsu Province Jianerkang Medical Dressing Co. ,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 34645-4001-4 5.5 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?

DirectionsClean the affected areaApply product on the area 1-3 times daily and discardMay be covered with a sterile bandage when dry DirectionsFor preparation of the skin prior to surgery* clean the affected area * remove swab by stick* apply to the operative site prior to surgeryFor use as a first aid antiseptic* clean the affected area* apply 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 UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Povidone-iodine?

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:

* Please review the disclaimer below.

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".