Zep Alcohol Sanitizer
Zep Alcohol Sanitizer is an FDA drug label for the active ingredient ETHANOL manufactured by Zep Inc. 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 20260813.
- Generic name
- ETHANOL
- Manufacturer
- Zep Inc.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 66949-133
- Application
- 505G(a)(3)
- Label effective
- 20260813
About this product
Zep Alcohol Sanitizer is an FDA-registered drug product whose active ingredient is ETHANOL. It is labelled by Zep Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 66949-133, application 505G(a)(3), label effective 20260813. It is one of 5 FDA drug label records sharing the active ingredient ETHANOL. 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 ETHANOL are most often described in connection with: hand sanitizing, decrease bacteria, skin rinsing. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Hand sanitizing to decrease bacteria on skin. No rinsing required.
Dosage & Administration
Directions Wet hands thoroughly with spray mist. Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles. Continue rubbing vigorously until hands are dry. No rinsing or toweling is required.
Warnings
Warnings For external use only. Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water. Flammable. Keep away from fire, flame or spark.
More products with the same ingredient
ETHANOLAFCO 5511 Sanifect E3
View labelFoaming Instant Hand Sanitizer with Aloe
View labelONID Wipe
View labeltazza 63% alcohol foam sanitizer
View labelHow products containing ETHANOL compare
FDA lists 5 drug label records with ETHANOL 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 |
|---|---|---|---|
| — | — | Zep Inc. | 2 |
| — | — | MCKESSON MEDICAL-SURGICAL INC. | 1 |
| — | — | ONID Technology Corp | 1 |
| — | — | Tazza Brands East, Inc. | 1 |
| — | — | — | — |
Frequently asked questions
What is Zep Alcohol Sanitizer used for?
Uses Hand sanitizing to decrease bacteria on skin. No rinsing required.
Who makes Zep Alcohol Sanitizer?
Zep Inc. is the labeler of record for Zep Alcohol Sanitizer. 5 FDA label records share the active ingredient ETHANOL, 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 Zep Alcohol 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 Zep Alcohol 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 ETHANOL?
Yes. 5 FDA drug label records list ETHANOL 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 Zep Alcohol 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.