Active Ingredient
Benzalkonium chloride.........0.13%
Sono Hand Sanitizer
FDA Label NDC 77677-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Advanced Ultrasound Solutions Inc. for the product Sono Hand Sanitizer (NDC 77677-001). 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, when using this product, stop use and ask a doctor, 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 Hand Sanitizer
Uses
- Hand sanitizer to help reduce bacteria on skin
- Recommended for repeated use
Warnings
For external use only
Do not use in ears or mouth
When Using This Product
Avoid contact with eyes. In case of contact, flush eyes with water.
Stop Use And Ask A Doctor
If redness or irritation develops and persists for more than 72 hours.
Keep Out Of Reach Of Children
Children should be supervised when using this product
Directions
- Apply a small amount onto hand, then spread on both hands
- Rub hands together until dry
Inactive Ingredients
Glycerin, PEG/PPG-18/18 Dimethicone, water, Organic Citrus Aurantium Bergamia Fruit Oil.
Principal Display Panel
NDC: 77677-001-02, 77677-001-19
SONO® HEALTHCARE
MADE IN USA
FOAMING HAND SANITIZER
WITH MOISTURIZER AND BERGAMOT ESSENTIAL OIL
Kills 99.99% of most common germs
1.7 FL OZ (50 ml)
18.60 FL OZ (550 ml)
Label (02)
Label (19)
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