Povidone-iodine Scrub Solution
FDA Label NDC 59050-559

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Changzhou Maokang Medical Products Co., Ltd for the product Povidone-iodine Scrub Solution (NDC 59050-559). 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 drug facts, active ingredient, purpose, use, 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

Drug Facts

Active Ingredient

Povidone-Iodine 7.5%w/w

Purpose

Antiseptic

Use

for antiseptic skin preparation

Do Not Use

  • if allergic to iodine 
  • do not use in the eye

Stop Use And Ask A Doctor If

  • redness,irritation,swelling or pain persist or increases
  • infection occurs

Keep Out Of Reach Of Children.

In case of accidental ingestion, seek professional assistance or consult a Poison Control Center immediately.

Avoid pooling beneath patient.

Directions

  • apply locally as needed

Other Information

  • 0.75% titratable iodine
  • for hospital or professional use only

Inactive Ingredients:

Anhydrous citric acid, Sodium dodecyl sulfate, Hydroxyethyl cellulose, Nonoxynol-10, Potassium iodide, Sodium hydroxide, Purified water

* Please review the disclaimer below.