MagiCare Premium Hand Sanitizing Wipes

ALCOHOL TOPICAL HUMAN OTC DRUG

MagiCare Premium Hand Sanitizing Wipes is an FDA drug label for the active ingredient ALCOHOL manufactured by MAGICARE TECH 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 20260810.

Generic name
ALCOHOL
Manufacturer
MAGICARE TECH CORP
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
85276-104
Application
505G(a)(3)
Label effective
20260810

About this product

MagiCare Premium Hand Sanitizing Wipes is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by MAGICARE TECH CORP taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85276-104, application 505G(a)(3), label effective 20260810. It is one of 582 FDA drug label records sharing the active ingredient 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 ALCOHOL are most often described in connection with: hand sanitizer, help reduce. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENT ETHYL ALCOHOL 75% PURPOSE ANTIMICROBIAL

Indications & Usage

USES HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.

Dosage & Administration

DIRECTIONS: STORAGE: STORE AT ROOM TEMPERATURE. DISPENSING: LIFT THE FRONT LID. OPEN PROTECTIVE SEAL. PULL OUT WIPE, RESEAL, AND CLOSETHE LID. USE : WIPE HANDS THOROUGHLY. DISPOSAL: DO NOT FLUSH.

Warnings

WARNINGS: FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. • FOR EXTERNAL USE ONLY. DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER. STOP USE AND CONSULT WITH A PHYSICIAN IF IRRITATION DEVELOPS AND LASTS FOR MORE THAN 72 HOURS. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

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How products containing ALCOHOL compare

FDA lists 582 drug label records with 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
— — Bath & Body Works, Inc. 79
— — Shenzhen Lantern Scicence Co.,Ltd. 66
— — Fourstar Group USA, Inc. 41
— — Church & Dwight Co., Inc. 33
— — Target Corporation 23

Frequently asked questions

What is MagiCare Premium Hand Sanitizing Wipes used for?
USES HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.

Who makes MagiCare Premium Hand Sanitizing Wipes?
MAGICARE TECH CORP is the labeler of record for MagiCare Premium Hand Sanitizing Wipes. 582 FDA label records share the active ingredient 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 MagiCare Premium Hand Sanitizing Wipes 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 MagiCare Premium Hand Sanitizing Wipes 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 ALCOHOL?
Yes. 582 FDA drug label records list 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 MagiCare Premium Hand Sanitizing Wipes 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.