Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 79117-070
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Emerge Technologies, Inc. for the product Hand Sanitizer (NDC 79117-070). 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, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- on open skin wounds
- do not inhale or ingest
- do not use on infants
Otc - When Using
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water
■Avoid contact with open skin ■ Do not inhale or ingest
Otc - Stop Use
Stop use and ask a doctor if skin irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping
Children under 6 years of age use only under adult supervision
Not recommended for infants
Other Information
- Store below 110F (43C)
- May discolor fabrics
Inactive Ingredients
Water (Aqua), Glycerin, Butylene Glyool, Carbomer, Aminomethyl
Propanol, Aloe Barbadensis Leaf Extract, Xanthan Gum
* Please review the disclaimer below.
