Active Ingredient
Alcohol 70%
Hand Sanitizer
FDA Label NDC 62583-020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Broncolin, S.a. De C.v for the product Hand Sanitizer (NDC 62583-020). 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, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
■ To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
Flammable. Keep away from fire & flame. For external use hands only
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
Stop Use And Ask A Doctor If
■ irritation or redness develops ■ conditions persist for more than 72 hours ■ redness is present
Keep Out Of Reach Of Children
In case of accidental ingestion, contact a doctor or Poison Control Center immediately.
Directions
■ Wet hands throughhly with product,and allow to dry without wiping ■ For children under 6, use only with adult supervision ■ Not recommended for infants
Other Information
■ Do not store above105°F ■ May discolor some fabrics ■ Harmful to wood finishes and plastics
Inactive Ingredients
carbomer, glycerin, triethanolamine, water
Package Label
Package Label (Lblhndsntzrgel)
* Please review the disclaimer below.
