WIPE OUT Antibacterial Wipes, Fresh Scent
WIPE OUT Antibacterial Wipes, Fresh Scent is an FDA drug label for the active ingredient BENZALKONIUM CHLORIDE manufactured by Jianerkang Medical 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 20231023.
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Jianerkang Medical Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 34645-0010
- Application
- 505G(a)(3)
- Label effective
- 20231023
About this product
WIPE OUT Antibacterial Wipes, Fresh Scent is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE. It is labelled by Jianerkang Medical Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 34645-0010, application 505G(a)(3), label effective 20231023. 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: decrease bacteria, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses To decrease bacteria on the skin that could cause disease
Dosage & Administration
Directions allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants
Warnings
Warnings For external use only When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin Stop use and ask a doctor if irritation and redness develops condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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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 WIPE OUT Antibacterial Wipes, Fresh Scent used for?
Uses To decrease bacteria on the skin that could cause disease
Who makes WIPE OUT Antibacterial Wipes, Fresh Scent?
Jianerkang Medical Co., Ltd is the labeler of record for WIPE OUT Antibacterial Wipes, Fresh Scent. 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 WIPE OUT Antibacterial Wipes, Fresh Scent 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 WIPE OUT Antibacterial Wipes, Fresh Scent 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 WIPE OUT Antibacterial Wipes, Fresh Scent 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.