Advanced Alcohol Gel Sanitizer
Advanced Alcohol Gel Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by Betco Corporation, 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 20260909.
- Generic name
- ALCOHOL
- Manufacturer
- Betco Corporation, Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 65601-801
- Application
- 505G(a)(3)
- Label effective
- 20260909
About this product
Advanced Alcohol Gel Sanitizer is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Betco Corporation, Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 65601-801, application 505G(a)(3), label effective 20260909. It is one of 582 FDA drug label records sharing the active ingredient 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.
What it is used for
Across FDA labelling, products containing ALCOHOL are most often described in connection with: hand sanitizer, reduce microorganisms. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Uses • Hand sanitizer to reduce microorganisms on the skin. • Use this product when soap and water are not available.
Dosage & Administration
Directions Directions • Read the entire label before using this product. • Place enough product on your palm to thoroughly cover your hands. • Rub hands together briskly until dry.
Warnings
Warnings Warnings • For external use only. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition. • Discontinue use if irritation or redness develops. • If irritation persists for more than 72 hours, consult a physician. • 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 ALCOHOL compare
FDA lists 582 drug label records with 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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Bath & Body Works, Inc. | 79 |
| — | — | Shenzhen Lantern Scicence Co.,Ltd. | 66 |
| — | — | Fourstar Group USA, Inc. | 41 |
| — | — | Church & Dwight Co., Inc. | 33 |
| — | — | Target Corporation | 23 |
Frequently asked questions
What is Advanced Alcohol Gel Sanitizer used for?
Uses Uses • Hand sanitizer to reduce microorganisms on the skin. • Use this product when soap and water are not available.
Who makes Advanced Alcohol Gel Sanitizer?
Betco Corporation, Ltd is the labeler of record for Advanced Alcohol Gel Sanitizer. 582 FDA label records share the active ingredient 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 Advanced Alcohol Gel 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 Advanced Alcohol Gel 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 ALCOHOL?
Yes. 582 FDA drug label records list 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 Advanced Alcohol Gel 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.