FDA.reportPublic FDA data

Ethyl Rubbing Alcohol

Manufacturer
Iron Lab SA de CV
Effective date
2026-02-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:46:01

Label at a glance#

ProductEthyl Rubbing Alcohol
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

91% Ethyl Alcohol

DOSAGE & ADMINISTRATION SECTION

Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

INSTRUCTIONS FOR USE SECTION

Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

INACTIVE INGREDIENT SECTION

Purified Water

OTC - STOP USE SECTION

Irritation or redness develops. Condition persist for more than 72 hours.

OTC - PURPOSE SECTION

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

WARNINGS SECTION

For external use only: hands. Flammable, Keep away from fire of flame.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - ASK DOCTOR SECTION

Irritation or redness develops. Condition persist for more than 72 hours.

OTHER SAFETY INFORMATION

Store below 105°F. May discolor some fabrics. Harmful to wood finishes and plastic

INDICATIONS & USAGE SECTION

Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ethyl Rubbing Alcohol 91Ethyl Rubbing Alcohol 91Ethyl Rubbing Alcohol 91

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2710539ethanol 91 % Topical SolutionPSN2
2710539ethanol 0.91 ML/ML Topical SolutionSCD2
2710539ethanol 91 % Topical SolutionSY2
2710539ethyl alcohol 91 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74375-020-01Ethyl Rubbing Alcohol355 mL in 1 BOTTLE, DISPENSINGLIQUID3552

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74375-02074375-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
Ethyl Rubbing AlcoholALCOHOLIron Lab SA de CV323b2f5d-34b9-8f5b-e063-6394a90a59d52026-02-17WarningsExact identifier
ndc (package): 74375-020-01
ndc (product): 74375-020
ndc11 (package): 74375002001
spl id: 4b08bd93-86a3-7061-e063-6294a90a29a9
spl set id: 323b2f5d-34b9-8f5b-e063-6394a90a59d5

Reported adverse events (FAERS/openFDA)#

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