meijer PUMPKIN SPICE SCENTED Hand Sanitizer

ETHYL ALCOHOL TOPICAL HUMAN OTC DRUG

meijer PUMPKIN SPICE SCENTED Hand Sanitizer is an FDA drug label for the active ingredient ETHYL ALCOHOL manufactured by Meijer, 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 20260430.

Generic name
ETHYL ALCOHOL
Manufacturer
Meijer, Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
79481-0089
Application
505G(a)(3)
Label effective
20260430

About this product

meijer PUMPKIN SPICE SCENTED Hand Sanitizer is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Meijer, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 79481-0089, application 505G(a)(3), label effective 20260430. It is one of 184 FDA drug label records sharing the active ingredient ETHYL 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 ETHYL ALCOHOL are most often described in connection with: decreases bacteria. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Ethyl Alcohol 70% v/v

Indications & Usage

Uses Decreases bacteria on skin.

Dosage & Administration

Directions • Adults and children 6 years and older Spray onto hands and rub them together until dry. Recommended for repeated use. • Children under 6 years of age Should be supervised when using this product.

Warnings

Warnings For external use only: hands Flammable, keep away from fire or flame. Do not use • If you are allergic to any of the ingredients. When using this product • Do not get into eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor • If irritation or rash develops and continues for more than 72 hours. Keep out of reach of children. If swallowed, call Poison Help at 1-800-222-1222 or go to PoisonHelp.org.

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How products containing ETHYL ALCOHOL compare

FDA lists 184 drug label records with ETHYL 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 formProductsManufacturerProducts
— — Diamond Life Cosmetics Trading FZCO 33
— — Ashtel Studios, Inc. 30
— — Amber Glow Cosmetics Limited 22
— — PEACH LAYNE, LLC 10
— — Apollo Health and Beauty Care 8

Frequently asked questions

What is meijer PUMPKIN SPICE SCENTED Hand Sanitizer used for?
Uses Decreases bacteria on skin.

Who makes meijer PUMPKIN SPICE SCENTED Hand Sanitizer?
Meijer, Inc. is the labeler of record for meijer PUMPKIN SPICE SCENTED Hand Sanitizer. 184 FDA label records share the active ingredient ETHYL 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 meijer PUMPKIN SPICE SCENTED Hand 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 meijer PUMPKIN SPICE SCENTED Hand 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 ETHYL ALCOHOL?
Yes. 184 FDA drug label records list ETHYL 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 meijer PUMPKIN SPICE SCENTED Hand 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.