Decon7 Antiseptic Foaming Hand Sanitizer
Decon7 Antiseptic Foaming Hand Sanitizer is an FDA drug label for the active ingredient BENZALKONIUM CHLORIDE manufactured by Decon7 Systems, LLC 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 20231016.
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Decon7 Systems, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 78245-201
- Application
- 505G(a)(3)
- Label effective
- 20231016
About this product
Decon7 Antiseptic Foaming Hand Sanitizer is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE. It is labelled by Decon7 Systems, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 78245-201, application 505G(a)(3), label effective 20231016. 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 sanitizing, decrease bacteria, skin recommended. 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 sanitizing to decrease bacteria on the skin Recommended for repeated use
Dosage & Administration
Directions Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry
Warnings
Warnings For external use only When using this product avoid contact with eyes. In case of eye contact, flush eyes thoroughly with water. Stop use and ask a doctor if irritation or redness develop or last 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 Decon7 Antiseptic Foaming Hand Sanitizer used for?
Uses For hand sanitizing to decrease bacteria on the skin Recommended for repeated use
Who makes Decon7 Antiseptic Foaming Hand Sanitizer?
Decon7 Systems, LLC is the labeler of record for Decon7 Antiseptic Foaming Hand Sanitizer. 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 Decon7 Antiseptic Foaming Hand Sanitizer 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 Decon7 Antiseptic Foaming Hand Sanitizer 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 Decon7 Antiseptic Foaming Hand Sanitizer 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.