Hand sanitizer 8oz with vitamin E
Hand sanitizer 8oz with vitamin E is an FDA drug label for the active ingredient ETHYL ALCOHOL 70% manufactured by REJOICE INTERNATIONAL 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 20260713.
- Generic name
- ETHYL ALCOHOL 70%
- Manufacturer
- REJOICE INTERNATIONAL CORP.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 57337-140
- Application
- M003
- Label effective
- 20260713
About this product
Hand sanitizer 8oz with vitamin E is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL 70%. It is labelled by REJOICE INTERNATIONAL CORP. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 57337-140, application M003, label effective 20260713. It is one of 30 FDA drug label records sharing the active ingredient ETHYL ALCOHOL 70%. 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 ETHYL ALCOHOL 70% are most often described in connection with: handwashing decrease, 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 handwashing to decrease bacteria on the skin recommended for repeated use
Dosage & Administration
Directions wet hands thoroughly with product briskly rub hands together until dry supervise children under 6 years in the use of this product
Warnings
Warnings For ecternal use only Flammable, keep away from heat and flame Do not use Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor Stop use and ask a doctor if irritation and redness develop and persist 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 ETHYL ALCOHOL 70% compare
FDA lists 30 drug label records with ETHYL ALCOHOL 70% 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 |
|---|---|---|---|
| — | — | MY IMPORTS USA LLC | 14 |
| — | — | Zhejiang Guoyao Jingyue Aerosol Co., Ltd. | 14 |
| — | — | REJOICE INTERNATIONAL CORP. | 2 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Hand sanitizer 8oz with vitamin E used for?
Uses for handwashing to decrease bacteria on the skin recommended for repeated use
Who makes Hand sanitizer 8oz with vitamin E?
REJOICE INTERNATIONAL CORP. is the labeler of record for Hand sanitizer 8oz with vitamin E. 30 FDA label records share the active ingredient ETHYL ALCOHOL 70%, 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 Hand sanitizer 8oz with vitamin E 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 Hand sanitizer 8oz with vitamin E 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 ETHYL ALCOHOL 70%?
Yes. 30 FDA drug label records list ETHYL ALCOHOL 70% 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 Hand sanitizer 8oz with vitamin E 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.