SurelyWell HAND SANITIZER Gel

Manufacturer
Surelywell, Inc.
Effective date
2021-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:57:52

Label at a glance#

ProductSurelyWell HAND SANITIZER Gel
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin. For use when soap and water are unavailable

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry. Children Under 6 years of age should be supervised by an adult when using.

Storage and handling

Do not store above 104°F/40°C

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol v/v 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin. For use when soap and water are unavailable

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

When using this product

Avoid contact with eyes, ears, and mouth.

If contact occurs, rinse thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if irritation and redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry. Children Under 6 years of age should be supervised by an adult when using.

Other information

STORAGE AND HANDLING SECTION

Do not store above 104°F/40°C

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Ammonium Polyacryloyldimethyl Taurate, Aloe Barbadensis Leaf Juice.

SPL UNCLASSIFIED SECTION

70% Alcohol

Distributed by and
Manufactured for:
SurelyWell, Inc
16192 Coastal Hwy
Lewes DE 19958

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

PackagingPackaging

Products#

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DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90094-06590094-065-04, 90094-065-08, 90094-065-98

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
ca6367fc-d8eb-1573-e053-2a95a90a4cf7eb715a12-22a3-48e2-aab0-2350a849ca182021-08-25WarningsExact identifier
spl set id: eb715a12-22a3-48e2-aab0-2350a849ca18

Reported adverse events (FAERS/openFDA)#

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