Ethyl Alcohol

Manufacturer
RESQUE1ST LLC
Effective date
2020-09-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:16:15

Label at a glance#

ProductEthyl Alcohol
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other Information: Store below 110°F (43°C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Uses • Hand sanitizer to help reduce bacteria on the skin.

Warnings:

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask doctor if redness or irritation develops & persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Centre right away.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry. Children under 6 years should be supervised when using this product.

STORAGE AND HANDLING SECTION

Other Information: Store below 110°F (43°C). May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aqua, Isopropyl Alcohol, Polysorbate 20, Carbomer, Triethanolamine, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Parfum, Lilial, Benzyl Salicylate, Linalool, Hexyl Cinnamal, Alpha-Isomethyl Ionone.

SPL UNCLASSIFIED SECTION

WHEN EVERY SECONDS COUNTS

Kills 99% of germs!

ResQue1st, LLC

www.resque1st.com

Clearwater, FL 33755

Made in USA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73762-070-082022-01-28C16284748780-1d6a99b39-6103-a426-e053-dadaa90af4c2ResQues1st Instant Hand Sanitizer

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73762-07073762-070-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e3b1aef0-4d8b-4b32-84c7-ad022a87c3f7a1875ab2-1d09-4852-e053-2a95a90a64b82020-09-02WarningsExact identifier
spl id: e3b1aef0-4d8b-4b32-84c7-ad022a87c3f7
spl set id: a1875ab2-1d09-4852-e053-2a95a90a64b8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.