Alcohol Prep Pad Medium
Alcohol Prep Pad Medium is an FDA drug label for the active ingredient ALCOHOL PREP PAD manufactured by Yangzhou Huanrui Medical Technology Co., Ltd administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260908.
- Generic name
- ALCOHOL PREP PAD
- Manufacturer
- Yangzhou Huanrui Medical Technology Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87993-101
- Application
- M003
- Label effective
- 20260908
About this product
Alcohol Prep Pad Medium is an FDA-registered drug product whose active ingredient is ALCOHOL PREP PAD. It is labelled by Yangzhou Huanrui Medical Technology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87993-101, application M003, label effective 20260908. It is one of 2 FDA drug label records sharing the active ingredient ALCOHOL PREP PAD. 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.
What it is used for
Across FDA labelling, products containing ALCOHOL PREP PAD are most often described in connection with: directions wipe, injection site. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Directions wipe injection site vigorously and discard
Dosage & Administration
Uses For preparation of skin prior to injection
Warnings
Warnings Flammable - keep away from fire or flame. For external use only. Flammable, keep away from fire or flame. Do Not Use with electrocautery procedures In the eyes Stop Use If Irritation or redness develops. If the condition persists for more than 72 hours, consult a doctor. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away
More products with the same ingredient
ALCOHOL PREP PADHow products containing ALCOHOL PREP PAD compare
FDA lists 2 drug label records with ALCOHOL PREP PAD 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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Changzhou Maokang Medical Products Co., Ltd. | 1 |
| — | — | Yangzhou Huanrui Medical Technology Co., Ltd | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Alcohol Prep Pad Medium used for?
Directions wipe injection site vigorously and discard
Who makes Alcohol Prep Pad Medium?
Yangzhou Huanrui Medical Technology Co., Ltd is the labeler of record for Alcohol Prep Pad Medium. 2 FDA label records share the active ingredient ALCOHOL PREP PAD, 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 Alcohol Prep Pad Medium 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 Alcohol Prep Pad Medium 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 ALCOHOL PREP PAD?
Yes. 2 FDA drug label records list ALCOHOL PREP PAD 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 Alcohol Prep Pad Medium 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.