Foaming Instant Hand Sanitizer with Aloe

ETHANOL TOPICAL HUMAN OTC DRUG

Foaming Instant Hand Sanitizer with Aloe is an FDA drug label for the active ingredient ETHANOL manufactured by MCKESSON MEDICAL-SURGICAL 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 20230605.

Generic name
ETHANOL
Manufacturer
MCKESSON MEDICAL-SURGICAL INC.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
68599-5205
Application
M003
Label effective
20230605

About this product

Foaming Instant Hand Sanitizer with Aloe is an FDA-registered drug product whose active ingredient is ETHANOL. It is labelled by MCKESSON MEDICAL-SURGICAL INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 68599-5205, application M003, label effective 20230605. It is one of 5 FDA drug label records sharing the active ingredient ETHANOL. 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 ETHANOL are most often described in connection with: mckesson foaming, hand sanitizer, moisturizers emollients. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Purpose Ethanol 70% .................................................... hand sanitizer

Indications & Usage

McKesson Foaming Hand Sanitizer with Aloe With Moisturizers & Emollients With Pump for frequent use.

Dosage & Administration

Directions Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels.

Warnings

Warnings For external use only. Flammable, keep away from fire or flame. When using this product avoid contact with eyes. In case of eye contact, flush with water for 15 minutes. Discontinue use and see a doctor if irritation occurs. Avoid contact with broken skin.

More products with the same ingredient

ETHANOL

AFCO 5511 Sanifect E3

Zep Inc. View label

ONID Wipe

ONID Technology Corp View label

Zep Alcohol Sanitizer

Zep Inc. View label

tazza 63% alcohol foam sanitizer

Tazza Brands East, Inc. View label

How products containing ETHANOL compare

FDA lists 5 drug label records with ETHANOL 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
— — Zep Inc. 2
— — MCKESSON MEDICAL-SURGICAL INC. 1
— — ONID Technology Corp 1
— — Tazza Brands East, Inc. 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.

RecallProductFirmClassStatusReported
D-0538-2025 PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21 Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250730
D-0540-2025 BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK. Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250730
D-0539-2025 EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-880-02. Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250730
D-0401-2025 Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile, Manufactured for: Sandoz Inc., Princeton, NJ 08540, Distributed by Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product of Canada, NDC 54643-5649-1 Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250507
D-0400-2025 Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01 Mckesson Medical-Surgical Inc. Corporate Office Class II Ongoing 20250507

Frequently asked questions

What is Foaming Instant Hand Sanitizer with Aloe used for?
McKesson Foaming Hand Sanitizer with Aloe With Moisturizers & Emollients With Pump for frequent use.

Who makes Foaming Instant Hand Sanitizer with Aloe?
MCKESSON MEDICAL-SURGICAL INC. is the labeler of record for Foaming Instant Hand Sanitizer with Aloe. 5 FDA label records share the active ingredient ETHANOL, 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 Foaming Instant Hand Sanitizer with Aloe 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 Foaming Instant Hand Sanitizer with Aloe 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 ETHANOL?
Yes. 5 FDA drug label records list ETHANOL 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 Foaming Instant Hand Sanitizer with Aloe 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.