Povidone Iodine
FDA Label NDC 49953-1893

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 49953-1893). 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, warnings, otc - keep out of reach of children, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Saturated with: 10% povidone-Iodine, 1% Titratable Iodine

Inactive Ingredient

Water

Dosage & Administration

1 Swabstick. Apply to procedure site as needed.

Indications & Usage

For professional and hospital use

Apply to procedure site as needed. discard after single use.

Warnings

For professional and hospital use.

For external use only.

Discard after single use.

If pain, irritation, redness or swelling occurs, discontinue use and consult a physician.

Otc - Keep Out Of Reach Of Children

Professional and Hosptial use.

Otc - Purpose

Apply to procedure site as needed.

Package Label.Principal Display Panel

Povidone-Iodine Swabstick (1's)

Saturated with: 10% povidone-Iodine, 1% titratable iodine.
Package Image (Iodineswabstick)

Package Image (Iodineswabstick)

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