Aplicare Povidone-iodine Scrub

Aplicare Povidone-iodine Scrub is an FDA-registered drug product whose active ingredient is POVIDONE-IODINE. It is labelled by Aplicare Products, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 52380-4802, application 505G(a)(3), label effective 20260902. 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.

Across FDA labelling, products containing POVIDONE-IODINE are most often described in connection with: skin preparation, patient preoperative. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use • antiseptic skin preparation • single use when used for patient preoperative skin preparation

Directions apply topically as needed

Warnings For external use only Avoid "pooling" beneath patient. Prolonged exposure to wet solution may cause skin irritation. Do not use in the eyes on individuals allergic or sensitive to iodine Ask a doctor before use if injuries are deep or puncture wounds serious burns Stop use and ask a doctor if infection occurs redness, irritation, swelling or pain persists or increases Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

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 Aplicare Povidone-iodine Scrub used for?
Use • antiseptic skin preparation • single use when used for patient preoperative skin preparation

Who makes Aplicare Povidone-iodine Scrub?
Aplicare Products, LLC is the labeler of record for Aplicare Povidone-iodine Scrub. 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 Aplicare Povidone-iodine Scrub 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 Aplicare Povidone-iodine Scrub 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 Aplicare Povidone-iodine Scrub 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.