Otc - Active Ingredient
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 73803-909
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Detergent Marketing Systems, Inc. for the product Hand Sanitizer (NDC 73803-909). 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 otc - active ingredient, otc - purpose, warnings, otc - when using, otc - keep out of reach of children, dosage & administration, indications & usage, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses: Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available
Warnings
Warnings: For external use only. Flammable. Keep away from heat and flame.
Otc - When Using
When using this product:
- Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
- Avoid contact with broken skin.
- Stop use and ask a doctor if skin irritation 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.
Dosage & Administration
Directions: Wet hands thoroughly with product and allow to dry without wiping
- For children under 6 years old, use only under adult supervision.
- Not recommended for infants.
Indications & Usage
Other Information:
- Do not store above 105 degree F
- May discolor some fabrics
- Harmful to wood finishes and plastics.
Inactive Ingredient
Inactive Ingredients: aloe vera, carbomer, glycerin, propylene glycol, water
* Please review the disclaimer below.
