ethanol

Manufacturer
Superior Chemical Co DBA NorthWoods | Betco Corp LLC
Effective date
2024-12-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:48:59

Label at a glance#

Productethanol
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to reduce microorganisms on the skin. Use this product when soap and water are not available

Dosage and administration

when using this product avoid contact with eyes. if contact occurs, rinsth thoroughly wiht water. Stop use and ask a doctor if irriataion or rash occurs

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% V/V

Warning statement

WARNINGS SECTION

Fore external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame

purpose

OTC - PURPOSE SECTION

Antiseptic

when using directions

OTC - WHEN USING SECTION

when using this product avoid contact with eyes. if contact occurs, rinsth thoroughly wiht water.

Stop use and ask a doctor if irriataion or rash occurs

inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juide, D&C Green #5, Fragrance, PER-10 Acrylate/perfluorohexylethly Acrylate copolymer, Perfluoroheexylethyl alcohol, propylene glycol, water

keep out of reach of children wording

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.

Directions for usage and dosage

DOSAGE & ADMINISTRATION SECTION

Read entire label before using this product

Place enough product on your palm to thoroughly cover your hands. Rub hands together briskly until dry

indications and usage

INDICATIONS & USAGE SECTION

Hand sanitizer to reduce microorganisms on the skin.

Use this product when soap and water are not available

principle label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product labelproduct label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53125-803-88ethanol500 mL in 1 BOTTLE, PLASTICSOAP5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53125-803ETHANOL (DERMA FOAM EXCEL HAND SANITIZER) SOAP [SUPERIOR CHEMICAL CO DBA NORTHWOODS]3Current NDC, 1 package rows20241228_26e26d6b-4f1a-46f7-e063-6394a90a3e7d.zip

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
53125-80353125-803-88

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
ethanolDERMA FOAM EXCEL HAND SANITIZERSuperior Chemical Co DBA NorthWoods26e26d6b-4f1a-46f7-e063-6394a90a3e7d2024-12-27WarningsExact identifier
ndc (package): 53125-803-88
ndc (product): 53125-803
ndc11 (package): 53125080388
spl id: 2a42de2e-7a70-3c01-e063-6294a90a3883
spl set id: 26e26d6b-4f1a-46f7-e063-6394a90a3e7d

Reported adverse events (FAERS/openFDA)#

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