Be Smart Get Prepared Hand Sanitizer

ALCOHOL TOPICAL HUMAN OTC DRUG

Be Smart Get Prepared Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by Total Resources International, 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 20260824.

Generic name
ALCOHOL
Manufacturer
Total Resources International, Inc
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
55550-611
Application
M003
Label effective
20260824

About this product

Be Smart Get Prepared Hand Sanitizer is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Total Resources International, Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 55550-611, application M003, label effective 20260824. 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: decrease bacteria, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients (in each gram) Alcohol 70% v/v

Indications & Usage

Use to decrease bacteria on the skin that could cause disease single 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. Flammable: keep away from fire or flame. When using product Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor if irritation or redness develops condition persists for more than 72 hours Keep out of the reach of children . If swallowed, get medical help or contact a Poison Control Center right away.

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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 Be Smart Get Prepared Hand Sanitizer used for?
Use to decrease bacteria on the skin that could cause disease single use

Who makes Be Smart Get Prepared Hand Sanitizer?
Total Resources International, Inc is the labeler of record for Be Smart Get Prepared Hand Sanitizer. 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 Be Smart Get Prepared 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 Be Smart Get Prepared 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 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 Be Smart Get Prepared 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.