Op First Aid Series Povidone Iodine Prep Pad Cloth
FDA Label NDC 72459-012

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Ori-power Medtech Co.,ltd. for the product Op First Aid Series Povidone Iodine Prep Pad (NDC 72459-012). 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 ingredients, purpose, use, warnings, do not use, stop use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Povidone Iodine 10% USP (equivalent to iodine 1%)

Purpose

Antiseptic

Use

  • Antiseptic for preparation of the skin.
  • First aid antiseptic to help prevent skin infection.

Warnings

For external use only.

Do Not Use

Avoid contact with eyes.If happens,rinse thoroughly with water.

Stop Use

In case of deep or puncture wounds or serious burns,and if pain,irritation, redness, swelling,or infection occurs,discontinue use and contact a physician.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a poison control center right away.

Directions

Clean intended area thoroughly with pad.discard after single use.

Other Information

Store at room temperature 15°C-30°C (59°F-86°F).

Inactive Ingredients

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

Package Labeling:

Bottle3 (Bottle3)

Bottle3 (Bottle3)

* Please review the disclaimer below.