Lightning X Prep Pad

Lightning X Prep Pad is an FDA-registered drug product whose active ingredient is ISOPROPYL ALCOHOL. It is labelled by Changzhou Maokang Medical Products Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 59050-120, application M003, label effective 20260507. It is one of 128 FDA drug label records sharing the active ingredient ISOPROPYL ALCOHOL. 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.

indication

dosage

warning

FDA lists 128 drug label records with ISOPROPYL ALCOHOL 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 Lightning X Prep Pad used for?
indication

Who makes Lightning X Prep Pad?
Changzhou Maokang Medical Products Co., Ltd. is the labeler of record for Lightning X Prep Pad. 128 FDA label records share the active ingredient ISOPROPYL ALCOHOL, 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 Lightning X Prep 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 Lightning X Prep 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 ISOPROPYL ALCOHOL?
Yes. 128 FDA drug label records list ISOPROPYL ALCOHOL 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 Lightning X Prep 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.