Active Ingredient
Ethyl Alcohol 70% v/v
Hand Sanitizer Gel
FDA Label NDC 58228-0691
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prostat First Aid Llc for the product Hand Sanitizer (NDC 58228-0691). 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(s), 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(S)
For hand washing to decrease bacteria on the skin
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 (1-800-222-1222) right away.
Directions
Wet hand thoroughly with product and allow to dry without wiping
Other Information
• Do not store above 110•F (43°C)
• May discolor some fabrics
• Recommended for repeated use
Inactive Ingredients
Aloe Vera Leaf Extract, Carbopol Ultrez 10, Fragrance, Glycerin, Propylene Glycol, Purified Water, Triethanolamine
Questions?
1-888-900-2920 Monday-Friday 8AM-4PM PST.
Label
Ps-0691_in_master (Ps 0691 In Master R231130 1)
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