Kleanerlab Hand Sanitizer

Manufacturer
Laboratorios Elizondo S.A. de C.V.
Effective date
2020-09-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:31

Label at a glance#

ProductKleanerlab Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

Place a small amount of gel in your palm and rub hands together until dry. For children under 6, use only under adult supervision. Not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only: hands.

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING 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. If skin irritation occurs seek medical advice.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place a small amount of gel in your palm and rub hands together until dry.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

  • Do not store above 110°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, USP Glycerin, Carbopol 940, Triethanolamine.

Package Labeling:250 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:1 L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80226-000-012022-01-28C16284748780-1d6a99b39-c9cf-a426-e053-dadaa90af4c2Kleanerlab Hand Sanitizer
80226-000-022022-01-28C16284748780-1d6a99b39-c9cf-a426-e053-dadaa90af4c2Kleanerlab Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80226-000-01Kleanerlab Hand Sanitizer250 mL in 1 BOTTLEGEL2501
80226-000-02Kleanerlab Hand Sanitizer1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80226-000KLEANERLAB HAND SANITIZER (ALCOHOL) GEL [LABORATORIOS ELIZONDO S.A. DE C.V.]1Legacy NDC, 2 package rows20200930_b073da58-7690-22d7-e053-2a95a90a9646.zip

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
80226-00080226-000-01, 80226-000-02

Ingredients#

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

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

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
b073daf5-f0f6-a140-e053-2a95a90a6954b073da58-7690-22d7-e053-2a95a90a96462020-09-29WarningsExact identifier
spl id: b073daf5-f0f6-a140-e053-2a95a90a6954
spl set id: b073da58-7690-22d7-e053-2a95a90a9646

Reported adverse events (FAERS/openFDA)#

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