Active Ingredients
Ethyl Alcohol 65% Antiseptic
Hallo Iceland Kelp Hand Sanitizer
FDA Label NDC 79655-495
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kala Corporation for the product Hallo Iceland Kelp Hand Sanitizer (NDC 79655-495). 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 ingredients, uses, warnings, when using this product, stop use and ask a doctor, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Sanitizer to help reduce bacteria on skin. For use when soap and water not available.
Sanitizer to help reduce bacteria on skin. For use when soap and water not available.
Warnings
For external use only. Keep away from heat or flame.
When Using This Product
Keep out of eyes. In case of contact, flush thoroughly with water. Avoid contact with broken skin.
Stop Use And Ask A Doctor
if irritation or rash occurs.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact Poison Control center right away.
Directions
Apply on hands, rub until dry.
Other Information
Store between 15-30C (58-86F) Avoid freezing and excess heat above 40C (104F)
Inactive Ingredients
Deionized Water, Acrylates Copolymer, Glycerin, PPG20 Methyl Glucose Ether, Fragrance Oil, Aminomethyl Propanol.
Package Label.Principal Display Panel
Moss (Moss)
Kelp (Kelp)
Ash (Ash)
Herb (Herb)
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