EthoGel

Manufacturer
HAYTHAM SCIENTIFIC LLC | HAITHAM ABDULRIDHA | HATHAM SCIENTIFIC LLC
Effective date
2020-12-19
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:01:02

Label at a glance#

ProductEthoGel
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


Ethyl alcohol 70% v/v Purpose: Antiseptic

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - DO NOT USE SECTION

Do not use • in children less than 2 months of age • on open skin wounds

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION


Use Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

OTC - STOP USE SECTION

Do not use • in children less than 2 months of age • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

DOSAGE & ADMINISTRATION SECTION


Directions
• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

WARNINGS SECTION


Warnings
For external use only. Flammable. Keep away from heat or flame

INACTIVE INGREDIENT SECTION

Inactive ingredients:

water, isopropyl alcohol, isopropyl myristate, glycerin, polyacrylate crosspolymer-6, alpha-tocopherol acetate, fragrance.

INDICATIONS & USAGE SECTION

Other information • Store between 15-30C (59-86F) • Avoid freezing and excessive heat above 40C (104F)

EthoGel label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236 mL NDC: 79270-0005-8236 mL NDC: 79270-0005-8236 mL NDC: 79270-0005-8236 mL NDC: 79270-0005-8

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79270-000579270-0005-8

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
ce68126e-6c28-9d64-e053-2a95a90afc8fa8cccf05-e197-23c8-e053-2a95a90ad68c2021-10-15WarningsExact identifier
spl set id: a8cccf05-e197-23c8-e053-2a95a90ad68c

Reported adverse events (FAERS/openFDA)#

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