Povidone-Iodine Pad

Povidone-Iodine Pad is an FDA-registered drug product whose active ingredient is POVIDONE-IODINE. It is labelled by Shandong Haiyan Medical Manufacture Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 42339-003, application M003, label effective 20220319. It is one of 58 FDA drug label records sharing the active ingredient POVIDONE-IODINE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Use Antiseptic for preparation of the skin.

Directions Apply locally as needed. Other Information Store at room temperature: 59°- 86°F(15 - 30℃)

Warnings For external use only. Discontinue use if irritation and redness develop. Keep out of reach of Children.

FDA lists 58 drug label records with POVIDONE-IODINE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Povidone-Iodine Pad used for?
Use Antiseptic for preparation of the skin.

Who makes Povidone-Iodine Pad?
Shandong Haiyan Medical Manufacture Co., Ltd. is the labeler of record for Povidone-Iodine Pad. 58 FDA label records share the active ingredient POVIDONE-IODINE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Povidone-Iodine Pad come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Povidone-Iodine Pad prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing POVIDONE-IODINE?
Yes. 58 FDA drug label records list POVIDONE-IODINE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Povidone-Iodine Pad been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.