FDA.reportPublic FDA data

Eclean Hand Sanitizer

Manufacturer
Eksa Mills, S.A. de C.V.
Effective date
2020-12-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:02:23

Label at a glance#

ProductEclean Hand Sanitizer
Active ingredientALCOHOL
Label structure8 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 Alcoho 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.

Do not use

OTC - DO NOT USE SECTION

  • 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

Water,Carbomer,Triethanolamine, Glycerin and Aloe vera

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77538-01077538-010-01, 77538-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
d7826fd0-96c3-cbe7-e053-2995a90a8510b631caa0-1366-040f-e053-2995a90abe652022-02-08WarningsExact identifier
spl set id: b631caa0-1366-040f-e053-2995a90abe65

Reported adverse events (FAERS/openFDA)#

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