Povidone-iodine Prep Pad
FDA Label NDC 80514-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Haida International Trading Co., Ltd. for the product Povidone-iodine Prep Pad (NDC 80514-002). 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 ingredient, purpose, caution: keep out of reach of children, use, warnings, directions, inactive ingredient, drug facts, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Povidone Iodine USP, 10% w/w

Purpose

Antiseptic

Caution: Keep Out Of Reach Of Children

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

Use

Antiseptic for preparation of the skin.

Warnings

For external use only.

Discontinue use if irritation and redness develop.

Directions

Open packet and use as a washcloth.

Inactive Ingredient

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

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