Active Ingredient
Ethyl Alcohol 70%
Sannytize Hand Sanitizer Gel
FDA Label NDC 67777-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Sannytize Hand Sanitizer (NDC 67777-010). 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, warnings, do not use, when using this product, stop use and ask a doctor if, 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
Antiseptic Handwash
Use
- For hand washing to decrease bacteria on the skin. Recommended for repeated use.
Warnings
For external use only
Flammable. Keep away from fire or flame
Do Not Use
in the eyes.
When Using This Product
avoid contact with eyes. In case of eye contact, rinse with water to remove.
Stop Use And Ask A Doctor If
irritation and redness develop.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Wet hands thoroughly with product and allow to dry without wiping
Other Information
- Do not store above 110°F
- May discolor some fabrics
Inactive Ingredients
Aloe Vera Leaf, Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked), Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water
* Please review the disclaimer below.
