Povidone-iodine Solution Sterile Liquid
FDA Label NDC 59050-554

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 Solution Sterile (NDC 59050-554). 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, use, do not use, stop use and ask a doctor if, keep out of reavh of children., ask a doctor before use if injuries are, 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 10%USP

Purpose

First aid 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 persists or increases
  • infection occurs

Keep Out Of Reavh Of Children.

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Avoid pooling beneath patient.

Ask A Doctor Before Use If Injuries Are

  • deep or punture wounds
  • serious burns

Directions

Apply product to skin as needed.

Other Information

  • 1% titratable iodine
  • for hospital or professional use only

Inactive Ingredients:

Citric Acid,Alkyl Glucoside,Hydroxyethyl cellulose,Nonoxynol-10,Glycerin,Sodium Hydroxide,Potassium Iodide, Purified Water.

Package Labeling:

Label (Label)

Label (Label)

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