Lights Povidone Iodine Scrub Solution
FDA Label NDC 61333-216

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Lights Medical Manufacture Co., Ltd. for the product Lights Povidone Iodine Scrub (NDC 61333-216). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - keep out of reach of children, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient: Povidone-Iodine USP: 7.5%

Otc - Purpose

Purpose: Antiseptic

Indications & Usage

Use:

antiseptic skin preparation

Warnings

Warnings:

Do not use if allergic to iodine

For external use only

Otc - Ask Doctor

Ask a doctor before use if injuries are

  • deep or puncture wounds
  • serious burns

    • Stop use and ask a doctor if

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

      • Do not use in eyes

      Avoid "pooling" beneath patient. Prolonged exposure to wet solution may cause skin irritation

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

Apply locally as need

Other Safety Information

Other information

  • 0.75% available iodine
  • latex free
  • for hospital or professional use only

Inactive Ingredient

Inactive Ingredient

disodium hudrogen phsophate, glycerol, ammonium dodecyl ether sulfate, hydroxyethylcellulose, water

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