Lights Povidone Iodine Prep Pad Solution
FDA Label NDC 61333-203

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 Prep Pad (NDC 61333-203). 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 - keep out of reach of children, otc - ask doctor, 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 (10%)

Otc - Purpose

Purpose: Antiseptic

Indications & Usage

Use:

First aid antiseptic to help prevent infection in minor cuts, scrapes and burns.

Warnings

Warnings:

For external use only

Do not use if allergic to iodine or in the eyes

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

Otc - Ask Doctor

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 if redness, irritation, swelling, or pain persists or increases

Dosage & Administration

Apply locally as need

Other Safety Information

Other information

  • 1% available iodine
  • latex free
  • for hospital or professional use only

Inactive Ingredient

Inactive Ingredient

Citric acid, purified water, Sodium phosphate dibasic

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Label (Lights)

Label (Lights)

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