Povidone-iodine
FDA Label NDC 53329-940

11 label sections · Submitted to the FDA by Medline Industries, Lp · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medline Industries, Lp for the product Povidone-iodine (NDC 53329-940). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Povidone-Iodine USP, 10%

Purpose

Antiseptic

Uses

  • First aid antiseptic to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do Not Use

  • in the eyes
  • longer than 1 week unless directed by a physician
  • on individuals who are allergic or sensitive to iodine
  • or apply over large areas of the body

Stop Use And Ask A Doctor If

  • irritation and redness develop
  • condition persists for more than 72 hours
  • in case of deep or puncture wounds, animal bites or serious burns

Keep Out Of Reach Of Children.

If swallowed, seek medical assistance or immediately contact a Poison Control Center.

Directions

  • clean the affected area
  • apply a small amount of this product on the area 1 to 3 times daily.
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other Information

  • do not flush
  • protect from freezing, avoid excessive heat

Inactive Ingredients

citric acid, disodium phosphate, purified water

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