Active Ingredient
Ethyl Alcohol 65%
Hand Sanitizer
FDA Label NDC 76781-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by S.f. & B. Color Mates Corp. for the product Hand Sanitizer (NDC 76781-001). 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, 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
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 heat or flame.
When Using This Product
■ Keep out of eyes. In case of contact with eyes, flush throughly with water. ■ Do not inhale or ingest. ■ Avoid contact with broken skin
Stop Use And Ask A Doctor If
if skin irritation develops.
Keep Out Of Reach Of Children
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
■ Wet hands thoroughly with product and allow to dry without wiping ■ For children under 6, use only under 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
Water, Glycerin, Carbomer, Aminomethylpropanol, Aloe Barbadensis Extract
Package Label
Package Label (Colormatehndsntzrlbl)
* Please review the disclaimer below.
