Maokang 10 Povidone Iodine Ointment
FDA Label NDC 59050-269

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 10 Povidone Iodine (NDC 59050-269). 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 nt use, ask a doctor before use, 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 USP 10%

Purpose

Antiseptic

Use:

First aid onitment, stop infection, no sting, antiseptic.

Warnings

  • For external use only.

Do Nt Use

  • if allergic to iodine or in the eyes.

Ask A Doctor Before Use

  • if injuries are deep wounds, puncture wounds, or serious burns. 

Stop Use And Ask A Doctor If

  • infection occurs or redness, irritation, swelling or pain persists or increases.

Keep Out Of Reach Of Children.

  • In case of accidental ingestion, seek professional assistance or consult a Poison Control Center immediately.
  • Avoid excessive heat. Store at room temperature.

Directions

apply locally as needed.

Other Information

  • 1%titratable iodine.
  • not made with natural rubber latex.
  • For hospital or professional use only.

Inactive Ingredients

Glycerin, PEG-1450, Propylene glycol, Hydroxyethyl Cellulose, Purified Water

Package Labeling:

Label00 (Label00)

Label00 (Label00)

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