Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 77720-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Skaffles Group Limited Liability Company for the product Hand Sanitizer (NDC 77720-006). 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, warning, otc - keep out of reach of children, directions, inactive ingredients, 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
Purpose
Antiseptic
Use
Hand sanitizing to help reduce bacteria on the skin.
Warning
For external use only. Flammable. Keep away from
When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
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
Squeeze a small amount in your palm
and briskly rub hands together until dry. Children
under 6 years of age should be supervised when in use
Inactive Ingredients
Water, Glycerol,Carbomer, Triethanolamine, Aloe.
* Please review the disclaimer below.
