NDC 0404-5639 Povidine Iodine

NDC Product Code 0404-5639

NDC CODE: 0404-5639

Proprietary Name: Povidine Iodine 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

  • 0404 - Henry Schein Inc

NDC 0404-5639-01

Package Description: 10 BOX in 1 CASE > 25 POUCH in 1 BOX > 3 POUCH in 1 POUCH > .9 mL in 1 POUCH

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

NDC Product Information

Povidine Iodine with NDC 0404-5639 is a product labeled by Henry Schein Inc. 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: 797730.

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.

  • NONOXYNOL-9 (UNII: 48Q180SH9T)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Henry Schein Inc
Labeler Code: 0404
Start Marketing Date: 03-17-2011 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: 12-31-2018 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.

Povidine Iodine 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

Otc - Active Ingredient

Active Ingredient                                  PurposePovidone Iodine 10% v/v                        Antiseptic

Uses:Povidone Iodine Swabstick 3

  • First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns.For preparation of the skin prior to surgery.Helps reduce bacteria that can potentially cause skin infections.



Do Not Use:

  • As a first aid antiseptic for more than 1 week.In the eyes.Over large areas of the body.

Ask A Doctor Before Use If You Have:

  • Deep puncture woundsAnimal bitesSerious burns

Stop Use:

  • If irritation and redness developIf condition persists for more than 72 hours, consult a physician.

Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center.


  • Tear at notch, remove applicator, use only once.As a first aid antisepticclean affected areaapply 1 to 3 times dailymay be covered with a sterile bandage, if bandaged let dry.For preoperative patient skin preparationclean areaapply to operative site prior to surgery using the applicator

Inactive Ingredient:Povidone_Iodine_Swabstick

Inactive Ingredient: Nonoxynol-9, Water

Indications & Usage

  • For use as an first aid antiseptic pre-operative skin preperation

* Please review the disclaimer below.