Active Ingredient
Ethyl Alcohol 68% v/v
Dr. Dris Hand Sanitizer
FDA Label NDC 81383-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hanson Venture Enterprise Inc for the product Dr. Dris Hand Sanitizer (NDC 81383-002). 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 - 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
Ethyl Alcohol 68% v/v................Antiseptic
Uses
Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.
Warnings
For external use only.
Flammable. Keep away from heat or flame.
Otc - Do Not Use
Do not use:
• on children less than 2 months of age
• on open skin wounds
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• place enough product on hands to cover all surfaces. Rub hands together until dry
• supervise children under 6 years of age when using this product to avoid swallowing
Other Information
• store in a cool dry place. Do not overheat.
Inactive Ingredients
Purified Water, Hydroxyethyl Cellulose, Coconut Pulp Extract, Lavender Oil, Eucalyptus Oil, Aloe Vera Leaf Juice,
* Please review the disclaimer below.
