FDA.reportPublic FDA data

Eclean solution advance hand sanitizer 70% Ethyl Alcohol

Manufacturer
EKSA MILLS S.A. DE C.V.
Effective date
2020-09-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:14:38

Label at a glance#

ProductEclean solution advance hand sanitizer 70% Ethyl Alcohol
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry. Children under six year of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

  • Flammable
  • Keep away from fire or flame

When using this product:

OTC - WHEN USING SECTION

  • Do not use in or near eyes. if contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

  • If irritation and redness persist for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek medical attention or contact a poison control center inmediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under six year of age should be supervised when using this product.

Other Information

SPL UNCLASSIFIED SECTION

  • store at 1°C-30°C(34°F- 86°F)

Inactive ingredientes:

INACTIVE INGREDIENT SECTION

Carbomer, Glycerin, Triethanolamine, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

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
77538-00777538-007-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
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
dd0671e1-4d6f-fb3c-e053-2995a90a1627af850b5e-c98a-3d4e-e053-2995a90a79482022-04-19WarningsExact identifier
spl set id: af850b5e-c98a-3d4e-e053-2995a90a7948

Reported adverse events (FAERS/openFDA)#

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