Active Ingredient
Ethyl Alcohol 70% v/v
Careall Hand Sanitizer Gel
FDA Label NDC 51824-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by New World Imports, Inc. for the product Careall Hand Sanitizer (NDC 51824-110). 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, otc - when using, otc - stop use, otc - 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
Hand sanitizer to help reduce bacteria on the skin that could cause disease
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a physician if skin irritation or rash develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If accidently ingested, seek medical help or contact a Poison Control Center immediately.
Directions
Place enough product in your palm to thoroughly cover your hands, rub together briskly until dry. Children under 6 years of age should be supervised when using this product.
Other Information
Store at normal room temperature. May discolor certain fabrics. May be harmful to wood finishes and plastics
Inactive Ingredients
Aloe Barbadenis Leaf Juice (Decolorized), Aminomethyl Propanol, Carbomer 980, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Mixed Tocopherol, Propylene Glycol, Purified Water,
* Please review the disclaimer below.
