Kleanerlab Hand Sanitizer
FDA Label NDC 80226-000

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Elizondo S.a. De C.v. for the product Kleanerlab Hand Sanitizer (NDC 80226-000). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

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

Warnings

For external use only: hands.

Flammable, keep away from fire or flame.

When Using This Product

  • 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.

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

Directions

  • 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

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

Inactive Ingredients

Water, USP Glycerin, Carbopol 940, Triethanolamine.

Questions Or Comments?

www.kleanerlab.com

Package Labeling:250 Ml

Label (Label)

Label (Label)

Package Labeling:1 L

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