Maokang Povidone Iodine Liquid
FDA Label NDC 59050-802

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 Maokang Povidone Iodine (NDC 59050-802). 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, warnings, do not use, ask a doctor before use if injuries are, stop use and ask a doctor if, 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 10%

Purpose

Antiseptic 

Use

  • Patient preoperative skin preparation: Helps to reduce bacteria that potentially can cause skin infection.

Warnings

  • For external use only.

Do Not Use

  • if allergic to iodine
  • in the eyes

Ask A Doctor Before Use If Injuries Are

  • deep wounds
  • puncture wounds
  • serious burns

Stop Use And Ask A Doctor If

  • infection occurs
  • redness, irritation or swelling develops

Keep Out Of Reach Of Children.

  • If swallowed, get medical help or contact a Poison Control Center right away

Other Information

  • 1% titratable iodine
  • Avoid excessive heat
  • Store at room temperature
  • For hospital or professional use only
  • Not madewith natural rubber latex

Inactive Ingredients

alkyl glucoside, citricacid, glycerin, hydroxyethyl cellulose, nonoxynol-10, potassium iodide, purified water, sodium hydroxide

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