Povidone Iodine
FDA Label NDC 49953-2805

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dalian Rongbang Medical Healthy Devices Co for the product Povidone Iodine (NDC 49953-2805). 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, inactive ingredient, dosage & administration, indications & usage, otc - keep out of reach of children, warnings, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

10% povidone-iodine solution equivalent to 1% available iodine.

Inactive Ingredient

not listed on label

Dosage & Administration

1 pad. for external use only

Indications & Usage

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

Otc - Keep Out Of Reach Of Children

for professional and hospital use.

Warnings



store at room temperature. In case of deep or puncture wounds or serious burns, and if pain, irritation, redness, swellling, or infection occurs, discontinue use and contact a physician. See drug facts panel on box. For external use only.

Otc - Purpose

Clean intended area.

Package Label.Principal Display Panel

Rongbang Antiseptic, Povidone-Iodine, USP, Prep Pad, Medium

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