FDA.reportPublic FDA data

70 Rubbing Ethyl 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 01:46:02

Label at a glance#

Product70 Rubbing Ethyl Alcohol
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

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

OTC - ACTIVE INGREDIENT SECTION

70 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.

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.

INACTIVE INGREDIENT SECTION

Purified Water

OTC - ACTIVE INGREDIENT SECTION

70% Ethyl Alcohol

OTC - STOP USE SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

OTC - PURPOSE SECTION

Antiseptic Alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70 Rubbing Alcohol70 Rubbing Alcohol70 Rubbing Alcohol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN2
1041849ethanol 0.7 ML/ML Topical SpraySCD2
1041849ethanol 70 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74375-050-0170 Rubbing Ethyl Alcohol355 mL in 1 BOTTLE, DROPPERLIQUID3552

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
74375-05074375-050-01

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
70 Rubbing Ethyl AlcoholALCOHOLIron Lab SA de CV323be8b4-4588-e2a6-e063-6394a90ab68b2026-02-17WarningsExact identifier
ndc (package): 74375-050-01
ndc (product): 74375-050
ndc11 (package): 74375005001
spl id: 4b08cc0e-f67a-9080-e063-6294a90a46af
spl set id: 323be8b4-4588-e2a6-e063-6394a90ab68b

Reported adverse events (FAERS/openFDA)#

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