Hand Sanitizer
FDA Label NDC 51706-508

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Landy International for the product Hand Sanitizer (NDC 51706-508). 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 otc - active ingredient, other safety information, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

​Drug Facts

​Active Ingredient

Ethyl Alcohol 63%

Purpose

Anticeptic

Other Safety Information

Other Information

  • Store at 68 o to 77 oF (20 o to 25 oc). 
  • Do not store above 105 oF. 
  • May discolor some fabrics. 
  • Harmful to wood finishes and plastics.

Package Label.Principal Display Panel

Label Image (Label)

Label Image (Label)

* Please review the disclaimer below.