ONID Wipe
ONID Wipe is an FDA drug label for the active ingredient ETHANOL manufactured by ONID Technology Corp 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 20170628.
- Generic name
- ETHANOL
- Manufacturer
- ONID Technology Corp
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 71441-180
- Application
- part333E
- Label effective
- 20170628
About this product
ONID Wipe is an FDA-registered drug product whose active ingredient is ETHANOL. It is labelled by ONID Technology Corp taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71441-180, application part333E, label effective 20170628. 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 washing, decrease bacteria, skin reccomended. 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 the skin Reccomended for repeated use
Dosage & Administration
Directions open packet remove and unfold wipe wipe hands throughly for approximately 15 seconds do not flush
More products with the same ingredient
ETHANOLAFCO 5511 Sanifect E3
View labelFoaming Instant Hand Sanitizer with Aloe
View labelZep Alcohol Sanitizer
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 ONID Wipe used for?
Uses For hand washing to decrease bacteria on the skin Reccomended for repeated use
Who makes ONID Wipe?
ONID Technology Corp is the labeler of record for ONID Wipe. 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 ONID Wipe 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 ONID Wipe 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 ONID Wipe 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.