Active Ingredient(S)
ETHYL ALCOHOL 68%
Hand Sanitizer Gel
FDA Label NDC 79805-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Juxin (jiangsu) New Material Packaging Co., Ltd. for the product Hand Sanitizer (NDC 79805-001). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, 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 and germs on the skin.
Recommendedfor repeated use
Warnings
For external use only-hands
Flammable. Keep away from heat and flame
Do Not Use
/
Otc - When Using
When using this product:Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a doctor if skin initation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children, In case of accidental ingestion, see professional assistance or contact a poison Control Center immediately.
Directions
Wet hands thoroughly with product and allow to dry wthout wiping.
For children under 6, use only under adult supervision
Not recommended for infants
Other Information
Do not store above 105°F
May discolor some fabrics
Harmful to wood finishes and plastics
Inactive Ingredients
Water(Aqua), Carbomer, Triethanolamine, Glycerin, Aloe vera, Vitamine E.
* Please review the disclaimer below.
