antibacterial wipes 01
antibacterial wipes 01 is an FDA drug label for the active ingredient BENZALKONIUM CHLORIDE manufactured by Cosmuses Cosmetics (Ningbo) 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 20260806.
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Cosmuses Cosmetics (Ningbo) Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 82953-072
- Application
- M003
- Label effective
- 20260806
About this product
antibacterial wipes 01 is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE. It is labelled by Cosmuses Cosmetics (Ningbo) Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82953-072, application M003, label effective 20260806. It is one of 231 FDA drug label records sharing the active ingredient BENZALKONIUM CHLORIDE. 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 BENZALKONIUM CHLORIDE are most often described in connection with: hand-washing decrease, bacteria skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For hand-washing to decrease bacteria on skin,
Dosage & Administration
Directions Slowly peel back label and use one wipe. Reseal, keep closed toprevent evaporation. Thoroughly wipe hands, allow to dry without rinsing. Discard after single use
Warnings
Warning For external use only. Do not use in eyes. In case of contact, rinse thoroughly with water. Stop use & ask doctor if rash/redness or irritation appears/developsand persist for more than 72 hours. Keep out of reach from children except under adult supervision.If swallowed, get medical help or contact a PoisonControl Center
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View labelHow products containing BENZALKONIUM CHLORIDE compare
FDA lists 231 drug label records with BENZALKONIUM CHLORIDE 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 |
|---|---|---|---|
| — | — | USA Broom LLC | 28 |
| — | — | Apollo Health and Beauty Care | 11 |
| — | — | Enviro Specialty Chemicals Inc | 11 |
| — | — | H E B | 10 |
| — | — | Jianerkang Medical Co., Ltd | 7 |
Frequently asked questions
What is antibacterial wipes 01 used for?
Uses For hand-washing to decrease bacteria on skin,
Who makes antibacterial wipes 01?
Cosmuses Cosmetics (Ningbo) Co., Ltd. is the labeler of record for antibacterial wipes 01. 231 FDA label records share the active ingredient BENZALKONIUM CHLORIDE, 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 antibacterial wipes 01 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 antibacterial wipes 01 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 BENZALKONIUM CHLORIDE?
Yes. 231 FDA drug label records list BENZALKONIUM CHLORIDE 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 antibacterial wipes 01 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.