Active Ingredient
Ethyl Alcohol 71%
Cleanze Hand Sanitizing
FDA Label NDC 77720-014
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 Cleanze Hand Sanitizing (NDC 77720-014). 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
For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use.
Warning
For external use only. Flammable. Keep away from fire or flame. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Discontinue use if irritation and redness develop. lf condition persists for more than 72 hours consult a physician.
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
Directions . Pump 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. Other information . Store between 15 and 30C(59 and 86F).ยท Avoid freezing and excessive heat above 40C(104F).
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Carbomer,Glycerin,Tocopheryl Acetate (Vitamin E), Triethanolamine, Water(Aqua).
* Please review the disclaimer below.
