FDA.reportPublic FDA data

ETHYL RUBBING ALCOHOL

Manufacturer
COMERCIALIZADORA JIQUILPAN S.A. DE C.V.
Effective date
2011-06-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:28:12

Label at a glance#

ProductETHYL RUBBING ALCOHOL
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

CONTAINS:70% Ethyl Alcohol by volume

as per label.jpg

OTC - PURPOSE SECTION

INDICATIONS. To decrease germs in minor cuts and scrapes

as per label.jpg

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS. Apply to skin directly or with clean gauze cotton or swab  For rubbing apply  liberally and rub with hands.

as per label.jpg

WARNINGS SECTION

WARNINGS.FOR EXTERNAL USE ONLY Will produce serious gastric disturbances if taken internally

as per label.jpg

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of accidental ingestion seek professional assistance or contact a Poison Control Center inmediately

as per label.jpg

INDICATIONS & USAGE SECTION

CAUTION Do not apply to irritated skin use in eyes or on mucous membranes incase of deep or puncture wounds consult a doctor

as per label.jpg

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS .Denatonium Benzoate water

as per label.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABELlabel. jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN3
582753ethanol 0.7 ML/ML Topical SolutionSCD3
582753ethanol 70 % Topical SolutionSY3
582753ethyl alcohol 70 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
15231-100-012019-10-29C16284748780-1960f7f55-d574-8e05-e053-dbdaa90a074aMAIN LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15231-100-01ETHYL RUBBING ALCOHOL500 mL in 1 BOTTLE, PLASTICLIQUID5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15231-100ETHYL RUBBING ALCOHOL (ALCOHOL) LIQUID [COMERCIALIZADORA JIQUILPAN S.A. DE C.V.]3Legacy NDC, 1 package rows20110607_990fd0fd-bb00-43e1-92d6-cbd0a532f012.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M3
ALCOHOLACTIVE MOIETY3K9958V90M3
DENATONIUM BENZOATE ANHYDROUSINACTIVE INGREDIENTM5BA6GAF1O3
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
15231-10015231-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT

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
add7f0ba-bb4c-4538-bedc-b1ab76c9199b990fd0fd-bb00-43e1-92d6-cbd0a532f0122011-06-05WarningsExact identifier
spl id: add7f0ba-bb4c-4538-bedc-b1ab76c9199b
spl set id: 990fd0fd-bb00-43e1-92d6-cbd0a532f012

Reported adverse events (FAERS/openFDA)#

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