Ethyl alcohol 62%
Ethyl alcohol 62% is an FDA drug label for the active ingredient ETHYL ALCOHOL 62% manufactured by UpLift Brands, 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 20260824.
- Generic name
- ETHYL ALCOHOL 62%
- Manufacturer
- UpLift Brands, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 83986-982
- Application
- 505G(a)(3)
- Label effective
- 20260824
About this product
Ethyl alcohol 62% is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL 62%. It is labelled by UpLift Brands, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83986-982, application 505G(a)(3), label effective 20260824. It is one of 2 FDA drug label records sharing the active ingredient ETHYL ALCOHOL 62%. 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 62% are most often described in connection with: decrease bacteria, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses to decrease bacteria on the skin that could cause disease recommended for repeated use
Dosage & Administration
Directions wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants
Warnings
Warnings For external use only: hands Flammable, keep away from fire or flame.
Adverse Reactions
Adverse Reaction Distributed by: UpLift Brands, LLC St. Louis, MO 63114 1-866 MY GERMX ^Fragrance name only
How products containing ETHYL ALCOHOL 62% compare
FDA lists 2 drug label records with ETHYL ALCOHOL 62% 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 |
|---|---|---|---|
| — | — | UpLift Brands LLC | 1 |
| — | — | UpLift Brands, LLC | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0105-2024 | Equate Hand Sanitizer (Ethyl Alcohol 62%), 7.5 FL.OZ. (221 mL) UPC 6 81131 05961 9 | Omega & Delta Co., Inc. | Class II | Ongoing | 20231122 |
| D-0098-2021 | Smart Care HAND SANITIZER, Ethyl Alcohol 62%, packaged in 0.84 FL.OZ (25 mL), labeled as a) Paw Patrol (Item #: 92321-144, UPC 8 50016 92321 9, NDC 70108-042-01); b) JoJo Siwa Dreamer (Item #: 92320-144, UPC 8 50016 92320 2, NDC 70108-044-01); c) Hot Wheels (Item #: 92317-144, UPC 8 50016 92317 2, NDC 70108-045-01); d) Barbie (Item #: 92318-144, UPC 8 50016 92318 9, NDC 70108-046-01); e) Trolls (Item #: 92322-144, UPC 8 50016 92322 6, NDC 70108-047-01); and f) Minions (Item #: 92319-144, UPC 8 50016 92319 6, NDC 70108-043-01); Distributed by Ashtel Studios Inc., Ontario, CA 91761 | ASHTEL STUDIOS, INC. | Class I | Terminated | 20201021 |
| D-1555-2020 | Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with Vitamin E, packaged in a) 16.9 Fl. Oz. (1.06 pint, 500 mL), NDC# 65055-600-02, UPC# 759684515033, b) 4 Fl. Oz.(120 mL), NDC# 65055-600-01, UPC# 75968455026, Laboratorios Jaloma S.A. DE C.V., Aquiles Serdan 438, Z.P. 44380, Guadalajara, Jalisco, Mexico, Made in Mexico. | Laboratorios Jaloma S.A. de C.V. | Class II | Terminated | 20200909 |
| D-1558-2019 | ICEE CHERRY SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102. | NingBo Huize Commodity Co.,Ltd. | Class III | Terminated | 20190807 |
| D-1550-2019 | TOOTSIE ROLL FRUIT CHEWS LIME SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102. | NingBo Huize Commodity Co.,Ltd. | Class III | Terminated | 20190807 |
Frequently asked questions
What is Ethyl alcohol 62% used for?
Uses to decrease bacteria on the skin that could cause disease recommended for repeated use
Who makes Ethyl alcohol 62%?
UpLift Brands, LLC is the labeler of record for Ethyl alcohol 62%. 2 FDA label records share the active ingredient ETHYL ALCOHOL 62%, 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 Ethyl alcohol 62% 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 Ethyl alcohol 62% 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 62%?
Yes. 2 FDA drug label records list ETHYL ALCOHOL 62% 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 Ethyl alcohol 62% been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
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.